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Why This Role MattersThe Physiotherapist at National 360 plays a vital role in delivering high-quality, community-based allied health services in Townsville. This position supports individuals with complex physical, neurological, intellectual, and psychosocial needs, empowering them to improve independence and overall quality of life within the NDIS framework.Job DescriptionNational 360 is seeking a passionate Physiotherapist for a Full-Time Permanent role based in Townsville, Queensland. The role offers a flexible caseload aligned with your clinical interests, hybrid work options (community, telehealth, clinic), structured professional development pathways, and strong multidisciplinary collaboration.Key Features of the Role• Position: Physiotherapist• Company: National 360• Location: Townsville (Aitkenvale Office), QLD• Employment Type: Permanent – Full Time• Salary: AU$83,200 per annum• Work Setting: Community, Telehealth & Clinic-Based• Client Focus: NDIS & Complex Care• Start: ImmediateResponsibilities• Manage a caseload tailored to your clinical interests (neurological, hydrotherapy, assistive technology, paediatrics, aged care, or generalist mix)• Deliver services via community visits, telehealth, and clinic sessions• Support individuals with physical disabilities, neurological conditions, intellectual disabilities, and psychosocial challenges• Empower and motivate clients to achieve meaningful functional outcomes• Collaborate with Occupational Therapists, Speech Pathologists, and Physiotherapists in a multidisciplinary team• Participate in supervision, mentoring, and structured career development programs• Maintain accurate documentation and compliance with NDIS standardsRequired Qualification• Relevant Tertiary Qualification in Physiotherapy• Current AHPRA RegistrationEducational Requirement• Recognised Physiotherapy degree in AustraliaImportant Requirements• Minimum 1+ year experience as a Physiotherapist• 1+ year experience working with NDIS clients (beneficial)• Full Australian working rights (no visa sponsorship available)• Current Driver’s Licence• Access to own vehicle• NDIS Workers Check (or willingness to obtain)• Blue Card (or willingness to obtain)Employment Options• Permanent Full-Time• Flexible scheduling• Hybrid model (Work-from-home + Office + Community visits)What We Offer• Competitive salary package• Generous Paid Parental Leave• 3 National 360 Days per year (for external PD or rest)• Up to 5 weeks annual leave via Purchased Leave Scheme• $1,500 annual Professional Development allowance• Structured Clinical & Operational Development Programs• 24/7 mental health & medical support via EAP (Sonder)• Fitness Passport & wellbeing initiatives• Discounted private health insurance & hospital excess coverage• Laptop & mobile phone provided• Regular peer supervision & specialist mentoring• Novated leasing options• Pet-friendly offices• Team-building events and celebration fundsExperience and Skills• Experience in neurological and musculoskeletal physiotherapy• Knowledge of NDIS frameworks and compliance• Strong assessment and treatment planning skills• Ability to manage community-based caseloads• Strong interpersonal and communication skills• Passion for improving client outcomesSalary Insights• AU$83,200 per annum• Additional benefits and professional development allowances included• Structured career progression pathwaysCompany OverviewFounded in 2006 by Heidi Long, National 360 is one of Australia’s leading community-based allied health providers, operating 22 offices across six states. As an NDIS-registered provider, the organisation delivers Occupational Therapy, Physiotherapy, Speech Pathology, Behaviour Support, and Early Childhood Intervention services, with a strong commitment to quality care and local community impact.FAQsWho can apply?Qualified Physiotherapists with at least 1 year of experience and Australian working rights.Is NDIS experience mandatory?Beneficial but not essential.Is visa sponsorship available?No, visa sponsorship is not offered for this role.What work model is offered?Hybrid – community visits, telehealth, and office-based work.How do I apply?Apply via the link below or contact Application Tips• Highlight your NDIS or complex care experience clearly.• Mention any special interest areas (neurology, hydrotherapy, paediatrics, assistive technology).• Demonstrate experience working independently in community settings.• Include measurable client outcome improvements if possible.• Clearly state your eligibility to work in Australia.

Why This Role MattersThe Physiotherapist at Priyanka's High Sky Child Development Center plays a vital role in supporting neurodiverse children through specialized pediatric physiotherapy interventions. This position focuses on improving motor skills, functional abilities, and overall development in children requiring individualized therapeutic care.Job DescriptionThe Pediatric Physiotherapist will work closely with neurodiverse children, providing tailored physiotherapy sessions to address developmental and neurological challenges. The role requires hands-on clinical expertise, patience, and a child-centric therapeutic approach in a full-time, on-site setting in Hyderabad.Key Features of the Role• Position: Physiotherapist• Company: Priyanka's High Sky Child Development Center• Location: Hyderabad, Telangana• Employment Type: Full-Time• Salary: ₹22,000 – ₹32,000 per month• Work Environment: In person (On-site)• Benefits: Provident Fund• Eligibility: Experienced Pediatric PhysiotherapistResponsibilities• Provide physiotherapy treatment to neurodiverse children• Develop individualized therapy plans based on assessment• Improve motor skills, posture, balance, and coordination• Monitor progress and modify treatment plans accordingly• Work collaboratively with caregivers and support staff• Maintain proper documentation of therapy sessionsRequired Qualification• Bachelor’s or Master’s degree in PhysiotherapyEducational Requirement• BPT or MPT from a recognized institutionImportant Remarks• Experience working with neurodiverse children is required• Full-time on-site role• Provident Fund benefits providedExperience and Skills• Strong pediatric physiotherapy expertise• Experience working with neurodiverse children• Good communication and interpersonal skills• Patience, empathy, and child-friendly approach• Ability to design customized therapy programsSalary Insights• ₹22,000 – ₹32,000 per month• Provident Fund benefits includedCompany OverviewPriyanka's High Sky Child Development Center in Hyderabad focuses on supporting children with developmental needs through specialized therapeutic services. The center provides structured and individualized interventions to enhance child development outcomes.FAQsWho can apply?Experienced Pediatric Physiotherapists with relevant qualifications.Is pediatric experience mandatory?Yes, experience working with neurodiverse children is required.What is the salary range?₹22,000 – ₹32,000 per month.What benefits are offered?Provident Fund.Where is the job located?Hyderabad, Telangana.Application Tips• Highlight pediatric and neurodiversity experience clearly in your CV• Mention specific therapy techniques used with children• Include certifications or specialized pediatric training if available

Why This Role MattersThe Physiotherapist at Kashi Spine Hospital plays a key role in delivering specialized spine and musculoskeletal rehabilitation services. This position supports patients in recovering from injuries, surgeries, and neurological conditions by providing structured, evidence-based physiotherapy care in Raipur, Chhattisgarh.Job DescriptionThe Physiotherapist will assess, diagnose, and treat patients with musculoskeletal and neurological conditions. The role involves developing personalized care plans, delivering rehabilitation programs, and collaborating with an interprofessional medical team. This is a full-time, permanent position suitable for freshers and candidates with up to 2 years of experience.Key Features of the Role• Position: Physiotherapist• Company: Kashi Spine Hospital • Location: Raipur, Chhattisgarh• Employment Type: Full-Time | Permanent• Salary: ₹11,300.38 – ₹29,389.92 per month• Work Environment: Hospital-based (In-person)• Eligibility: DPT / BPT• Experience: Fresher – 2 yearsResponsibilities• Conduct patient assessment and diagnose movement dysfunctions• Evaluate range of motion, strength, mobility, and functional abilities• Develop personalized, evidence-based treatment and care plans• Deliver therapeutic exercises, manual therapy, and use specialized equipment• Manage post-surgical, musculoskeletal, and neurological rehabilitation• Educate patients on posture correction, safe movement, and injury prevention• Collaborate with doctors and healthcare professionals for coordinated care• Maintain accurate documentation and patient progress recordsRequired Qualification• Diploma in Physiotherapy (DPT) or Bachelor of Physiotherapy (BPT)Educational Requirement• DPT / BPT from a recognized institutionImportant Remarks• Suitable for freshers and candidates with up to 2 years of experience• Exposure to musculoskeletal and neurological rehabilitation• In-person hospital-based roleExperience and Skills• Ability to create structured care plans• Strong assessment and diagnostic skills• Knowledge of therapeutic exercises and manual techniques• Good communication and patient counseling skills• Team collaboration and coordination abilityAge Eligibility• Not specifiedSalary Insights• ₹11,300.38 – ₹29,389.92 per month• Salary may vary based on experience and skill levelCompany OverviewKashi Spine Hospital is a specialized healthcare facility in Raipur, Chhattisgarh, focused on spine care, musculoskeletal treatment, and rehabilitation services. The hospital provides comprehensive physiotherapy and collaborative medical care to support patient recovery and long-term health.FAQsWho can apply?Candidates with DPT or BPT qualification (Freshers to 2 years experience).What is the salary range?₹11,300.38 – ₹29,389.92 per month.What type of job is this?Full-time and Permanent.Is this an in-person role?Yes, it is a hospital-based in-person role.What experience is required?Fresher to 2 years.Application Tips• Highlight your experience in developing care plans and patient assessments.• Mention any exposure to musculoskeletal or neurological rehabilitation.• Clearly state your qualification (DPT/BPT) and years of experience.• Include details of clinical postings or hospital training if you are a fresher.

Why This Role MattersThe Senior Physiotherapist (MPT) at Physiocares – Rapid Recovery Team plays a crucial role in delivering high-quality patient-centered rehabilitation services. This position ensures effective treatment planning, smooth clinic operations, and compassionate care for patients in Nikol, Ahmedabad.Job DescriptionPhysiocares is hiring a Senior Physiotherapist with a minimum of 3 years of professional experience to manage patient consultations, develop treatment plans, and oversee daily clinic operations. This is a freelance / contractual role requiring independent clinic management and strong patient-handling skills.Key Features of the Role• Position: Senior Physiotherapist (MPT)• Company: Physiocares – Rapid Recovery Team• Location: Nikol, Ahmedabad, Gujarat• Employment Type: Freelance | Contractual / Temporary• Salary: ₹10,000 – ₹40,000 per month• Work Environment: Clinic-based (In-person)• Experience Required: Minimum 3 years• Eligibility: MPT preferredResponsibilities• Conduct detailed patient consultations and assessments• Develop accurate and personalized treatment plans• Provide compassionate and professional patient care• Manage OPD and maintain proper case records• Monitor patient progress and provide follow-up guidance• Oversee day-to-day clinic operations• Coordinate appointments, reports, and patient support activities• Maintain a positive, empathetic clinic environmentRequired Qualification• Master of Physiotherapy (MPT) preferred• (As mentioned in the job post: BHMS degree from a recognized institution)Educational Requirement• Relevant degree from a recognized institutionImportant Remarks• Minimum 3 years of professional experience required• Ability to independently manage clinic activities• Freelance engagement model• In-person roleExperience and Skills• Strong physiotherapy and rehabilitation knowledge• Good understanding of medical terminology and physiology• Excellent communication and patient-handling skills• Strong decision-making and problem-solving abilities• Professional, friendly, and empathetic attitude• Capability to manage clinic operations independentlySalary Insights• ₹10,000 – ₹40,000 per month• Salary may vary based on experience, patient load, and skill levelCompany OverviewPhysiocares – Rapid Recovery Team is a rehabilitation-focused clinic located in Nikol, Ahmedabad, Gujarat. The clinic emphasizes rapid recovery programs, compassionate care, and efficient clinic management to provide quality physiotherapy services.FAQsWho can apply?Candidates with relevant physiotherapy qualifications and minimum 3 years of experience.What is the salary range?₹10,000 – ₹40,000 per month.What type of job is this?Freelance / Contractual role.Is prior experience mandatory?Yes, minimum 3 years of professional experience is required.Where is the job located?Nikol, Ahmedabad, Gujarat.Application Tips• Highlight your 3+ years of clinical experience clearly at the top of your resume.• Mention your experience in OPD management and clinic operations.• Emphasize independent decision-making and patient care experience.• Clearly state your qualification (BPT/MPT) and current location.

Why This Role MattersThe Physiotherapist (MPT – Cardio) at Physiocares – Rapid Recovery Team plays a key role in delivering personalized physiotherapy care to patients with physical challenges. This position focuses on home-visit rehabilitation services, ensuring patients receive quality treatment and support in the comfort of their homes in the Bopal area of Ahmedabad.Job DescriptionPhysiocares – Rapid Recovery Team is urgently hiring a qualified MPT Physiotherapist for home-visit services. The role involves assessing patients, facilitating treatment and therapy sessions, and supporting rehabilitation plans. This is a full-time, in-person position suitable for candidates with 0–1 year of experience.Key Features of the Role• Position: Physiotherapist (MPT – Cardio)• Company: Physiocares – Rapid Recovery Team• Location: Nikol, Ahmedabad, Gujarat (Home Visit – Bopal Area)• Employment Type: Full-Time• Salary: Up to ₹20,000 per month• Work Environment: Home Visit (In-person)• Experience Required: 0–1 year• Eligibility: MPT requiredResponsibilities• Conduct patient assessments during home visits• Facilitate treatment and therapy sessions for physical rehabilitation• Develop and implement appropriate therapy plans• Build and maintain rapport with patients• Monitor patient progress and provide necessary guidance• Maintain proper documentation and administrative records• Coordinate with team members for effective patient careRequired Qualification• Master of Physiotherapy (MPT) – MandatoryEducational Requirement• MPT from a recognized institutionImportant Remarks• Home visit role (Bopal Area)• Suitable for freshers and candidates with up to 1 year of experience• Good physical fitness required• Immediate joining preferredExperience and Skills• Basic physiotherapy and rehabilitation knowledge• Strong interpersonal and communication skills• Ability to build patient rapport• Teamwork and coordination skills• Basic administrative and documentation skills• Patience, tolerance, and professional attitudeSalary Insights• Up to ₹20,000 per month• Salary may vary based on experience and performanceCompany OverviewPhysiocares – Rapid Recovery Team is a rehabilitation-focused clinic based in Nikol, Ahmedabad, Gujarat. The clinic provides physiotherapy services including home-visit care, focusing on rapid recovery programs and patient-centered rehabilitation support.FAQsWho can apply?Candidates with MPT qualification (0–1 year experience).What is the salary offered?Up to ₹20,000 per month.Is prior experience mandatory?No, freshers with MPT can apply.What type of job is this?Full-time, home-visit role.Where is the service area?Bopal Area, Ahmedabad (Clinic based in Nikol).Application Tips• Clearly mention your MPT qualification at the top of your resume.• Highlight any internship or clinical exposure during your studies.• Mention your willingness to perform home visits.• Include your current location and immediate availability.

Why This Role MattersThe Senior General Dentist plays a crucial leadership role in delivering comprehensive dental care while maintaining high clinical standards and mentoring junior dentists. At Star Dental Centre Private Limited, this position ensures quality treatment delivery, patient satisfaction, and adherence to infection control protocols within a structured clinical environment.Job DescriptionStar Dental Centre Private Limited is hiring a Full-Time Senior General Dentist for its Bhayandar (Mumbai) location. The ideal candidate will have 5+ years of clinical experience and be proficient in advanced general dentistry procedures, treatment planning, and team mentorship.Key Features of the Role• Position: Senior General Dentist• Company: Star Dental Centre Private Limited• Location: Bhayandar, Mumbai, Maharashtra• Employment Type: Full-Time• Salary: ₹30,000 – ₹45,938.76 per month• Work Setting: In-Clinic (On-site)• Experience Required: 5+ Years• Start: ImmediateResponsibilities• Diagnose dental conditions and develop comprehensive treatment plans• Perform fillings, RCTs, extractions, crowns and bridges, scaling and polishing• Manage dental emergencies effectively• Ensure strict infection control and clinical compliance• Mentor junior dentists and support overall clinical quality• Maintain accurate patient records and documentationRequired Qualification• BDS / DDS degree• Valid Dental Council LicenseEducational Requirement• Recognised BDS or DDS degree from an accredited institutionImportant Requirements• Minimum 5+ years of clinical experience• Strong clinical expertise in advanced general dentistry• Excellent patient communication skills• Ability to manage complex treatment cases• Leadership and mentoring capabilitiesEmployment Options• Full-Time Position• Permanent Clinical Role• On-site PracticeWhat We Offer• Competitive monthly salary• Health insurance• Paid sick leave• Provident Fund benefits• Professional work environment• Opportunity to mentor and lead junior cliniciansExperience and Skills• Advanced general dentistry procedures (RCT, crowns, bridges, surgical extractions)• Strong treatment planning and case management• Clinical leadership and mentoring skills• Excellent communication and interpersonal skills• Strong infection control and compliance knowledgeSalary Insights• ₹30,000 – ₹45,938.76 per month• Additional employee benefits included• Salary based on experience and expertiseCompany OverviewStar Dental Centre Private Limited is a dental healthcare provider located in Bhayandar, Mumbai, offering comprehensive dental services with a focus on quality care and patient satisfaction. The clinic emphasizes advanced procedures, infection control compliance, and team-based clinical excellence.FAQsWho can apply?BDS/DDS-qualified dentists with 5+ years of experience and valid registration.Is this a full-time role?Yes, it is a full-time in-clinic position.What procedures are expected?RCTs, crowns, bridges, extractions, scaling, and advanced general dentistry procedures.Are employee benefits provided?Yes, including health insurance, paid sick leave, and provident fund.How do I apply?Apply through the link below.Application Tips• Clearly highlight your 5+ years of clinical experience.• Mention advanced procedures you are proficient in (RCT, crowns, bridges, etc.).• Emphasise leadership or mentoring experience.• Include patient communication strengths in your CV.• Keep your resume clinically focused and achievement-based.

Why This Role MattersThe Dental Assistant (Fresher) plays an important supporting role in ensuring smooth clinical operations and quality patient care. This position offers hands-on exposure to dental procedures while helping maintain patient comfort and efficient workflow within the clinic environment.Job DescriptionEaspire Technolabs Pvt Ltd (Posted by Evoke HR) is hiring a Full-Time Dental Assistant (Fresher) for Mumbai, Maharashtra. This opportunity is ideal for motivated freshers interested in dental care, patient interaction, and gaining practical clinical experience.Key Features of the Role• Position: Dental Assistant (Fresher)• Company: Easpire Technolabs Pvt Ltd• Posted By: Evoke HR• Location: Mumbai, Maharashtra• Employment Type: Full-Time, Permanent• Salary: Not Disclosed• Industry: Recruitment / Staffing• Department: Healthcare & Life Sciences• Experience: 0–1 Year• Openings: 1Responsibilities• Assist dentists during dental procedures by preparing instruments and materials• Ensure patient comfort before, during, and after treatments• Sterilize and organize dental instruments and equipment• Maintain accurate patient records and documentation• Schedule appointments and manage patient follow-ups• Support smooth day-to-day clinic workflowRequired Qualification• BDS – Bachelor of Dental Surgery (Dentistry / Orthodontics)Educational Requirement• Undergraduate Degree: BDS in Dentistry / OrthodonticsImportant Requirements• Basic knowledge of dental procedures and instruments• Good communication and interpersonal skills• Attention to detail and organizational ability• Ability to work in a fast-paced clinical environment• Empathy and patient-focused attitude• Willingness to learn under senior dentistsWhat We Offer• Entry-level opportunity for freshers• Practical clinical exposure• Professional healthcare work environment• Opportunity to develop dental assisting skillsExperience and Skills• 0–1 year experience (Freshers eligible)• Knowledge of dentistry, oral care, orthodontics• Strong communication skills• Organizational and record-keeping ability• Patient management capabilitySalary Insights• Salary: Not Disclosed• May vary based on company standards and candidate profileCompany OverviewEaspire Technolabs Pvt Ltd is a leading IT Outsourcing and Business Consulting company established over a decade ago. The organization focuses on business innovation through technology, business automation, software development, and Business Process Management services.FAQsWho can apply?Candidates with BDS qualification (Dentistry / Orthodontics), including freshers.Is prior experience required?No, this is open for freshers (0–1 year).What is the job location?Mumbai, Maharashtra.Is this a permanent role?Yes, it is a full-time permanent position.What skills are important?Basic dental knowledge, communication skills, organization, and willingness to learn.Application Tips• Mention your BDS specialization clearly in your resume.• Highlight any internship or clinical exposure experience.• Emphasize communication and patient-handling skills.• Keep your resume concise and structured.

Why This Role MattersThe General Dentist plays a vital role in delivering high-quality oral healthcare services to patients in Kanchipuram. At Apollo Dental, this role ensures patients receive accurate diagnosis, effective treatment, and education on preventive dental care while maintaining high clinical and infection control standards.Job DescriptionApollo Dental is hiring a Full-Time General Dentist for its Kanchipuram clinic. The role involves diagnosing and treating dental conditions, performing routine and advanced procedures, maintaining patient records, and ensuring adherence to infection control protocols. The clinic operates with structured shifts and provides a professional team-based work environment.Key Features of the Role• Position: General Dentist• Company: Apollo Dental• Location: Kanchipuram, Tamil Nadu• Employment Type: Full-Time• Salary: ₹20,000 – ₹35,000 per month• Work Setting: In-Clinic (On-site)• Shift Timing: 10:00 AM – 8:00 PM or 11:00 AM – 9:00 PM• Start: ImmediateResponsibilities• Diagnose and treat dental problems• Perform routine dental procedures including fillings, extractions, scaling, and RCT• Educate patients on oral hygiene and preventive dental care• Maintain accurate and updated patient records• Follow strict infection control and clinical standards• Work collaboratively with the clinic teamRequired Qualification• BDS (Bachelor of Dental Surgery)• Valid State Dental Council RegistrationEducational Requirement• Recognised BDS degree from an accredited institutionImportant Requirements• Good communication skills• Strong patient-handling abilities• Willingness to work in a team environment• Commitment to maintaining clinical standardsEmployment Options• Full-Time Position• Fixed clinic-based schedule• In-person work settingWhat We Offer• Competitive industry-standard salary• Structured clinic timings• Professional work environment• Opportunity to work with an established dental brand• Exposure to diverse patient casesExperience and Skills• Strong clinical diagnosis skills• Hands-on experience in general dentistry procedures• Good communication and interpersonal skills• Ability to manage patients effectively• Teamwork and professional attitudeSalary Insights• ₹20,000 – ₹35,000 per month• Based on experience and performance• As per industry standardsCompany OverviewApollo Dental is a leading dental healthcare provider in India, offering comprehensive dental treatments with modern infrastructure and standardized clinical protocols. The Kanchipuram branch is located at 12/70, Vallal Pachaiyappan Street, opposite Reliance Digital, Tamil Nadu 631501, delivering quality dental care to the local community.FAQsWho can apply?BDS-qualified dentists with valid registration.Is this a full-time role?Yes, this is a full-time, in-clinic position.What is the salary range?₹20,000 – ₹35,000 per month.What are the working hours?10 AM – 8 PM or 11 AM – 9 PM.How do I apply?Apply through the official careers page link below.Application Tips• Clearly mention your BDS qualification and registration details.• Highlight hands-on experience in RCT, extractions, and scaling.• Emphasise strong communication and patient-handling skills.• Mention your availability for full-time shifts.• Keep your resume concise and procedure-focused.

Why This Role MattersResearch fellowships are the foundation of innovation in science and technology. As a Junior Research Fellow at Birla Institute of Technology and Science Pilani (BITS Pilani), you will contribute to high-impact academic research under expert faculty supervision.This role offers advanced research exposure, hands-on experimentation, and analytical problem-solving opportunities. It is particularly valuable for candidates planning to pursue a Ph.D., academic research career, or industry R&D roles.Job DescriptionThe Junior Research Fellow (JRF) will assist in executing a sponsored research project. The role involves conducting experiments, data collection and analysis, literature review, documentation, and reporting.The selected candidate will work closely with the Principal Investigator (PI) and research team to ensure timely completion of project milestones. Depending on the project domain, responsibilities may include laboratory research, computational modeling, formulation development, analytical testing, or interdisciplinary collaboration.The position demands strong subject knowledge, research aptitude, and the ability to work systematically within project timelines.Key Features of the Role:• Opportunity to work in a reputed private deemed university• Exposure to funded research projects• Hands-on laboratory or technical research experience• Competitive fellowship amount• Strong academic and research career pathway• Collaborative research environmentResponsibilities• Assist in research project planning and execution• Conduct laboratory experiments or technical analyses• Perform literature review and data interpretation• Maintain research records and documentation• Prepare progress reports and presentations• Support manuscript drafting and publication activities• Ensure compliance with research and safety guidelines• Participate in project meetings and discussions• Complete assigned tasks within project deadlinesRequired Qualifications• M.E. / M.Tech• M. Pharm• M.ScEducational Requirements:Postgraduate degree in Engineering, Pharmacy, Science, or related discipline from a recognized university. Academic background must be relevant to the project domain.Experience and Skills:Technical Competencies:• Strong subject knowledge in relevant specialization• Research methodology understanding• Laboratory handling or analytical skills• Data analysis and interpretation capabilityCore Skills:• Analytical thinking and problem-solving ability• Good communication and documentation skills• Ability to work independently and in teams• Attention to detail• Time management and task prioritizationAge Eligibility:• Minimum Age: 21 Years• Maximum Age: 45 Years• Age relaxation applicable as per organization normsSalary Insights:• Monthly Fellowship: ₹37,000/-Remuneration will be provided as per project and institutional norms.Important Dates:• Starting Date of Application: 27-02-2026• Closing Date of Application: 10-03-2026Organization OverviewBirla Institute of Technology and Science Pilani (BITS Pilani) is a premier private deemed university in India known for excellence in engineering, science, pharmacy, and research innovation. The institute promotes interdisciplinary research, academic rigor, and industry collaboration.Working as a JRF at BITS Pilani provides exposure to advanced research infrastructure, experienced faculty mentorship, and a strong academic ecosystem.FAQsQ1: Is this a permanent position?No, this is a project-based contractual position.Q2: Is prior research experience mandatory?Not always mandatory, but research exposure is advantageous.Q3: Is the salary fixed?Yes, ₹37,000/- per month as per project norms.Q4: Can candidates from different specializations apply?Yes, provided the specialization matches the project requirement.Q5: Is age relaxation applicable?Yes, as per organization norms.Application Tips• Clearly mention your postgraduate specialization• Highlight thesis work and research exposure• Include technical and analytical skills in CV• Attach relevant certificates and documents• Submit application before 10-03-2026Official Notification Click Here

Why This Role MattersResearch scientists are central to transforming scientific knowledge into practical applications that benefit society. A Project Research Scientist at Jadavpur University contributes to cutting-edge research initiatives, strengthening innovation in pharmaceutical sciences and related disciplines.This role offers an opportunity to apply advanced pharmacological knowledge, conduct meaningful research, and collaborate with academic experts in a reputed public university. For candidates aiming to pursue doctoral research, industry R&D, or academic careers, this position provides valuable research exposure and professional development.Job DescriptionThe Project Research Scientist will work on an externally funded or university-supported research project. The role involves planning and executing research activities, data collection and analysis, maintaining laboratory records, and preparing technical reports.The selected candidate will assist the Principal Investigator (PI) in implementing the research methodology, managing documentation, and ensuring adherence to institutional research standards. Responsibilities may include laboratory experimentation, formulation development, pharmacological evaluation, statistical analysis, and report preparation depending on the project scope.The position requires strong scientific knowledge, research aptitude, and the ability to work independently within defined project timelines.Key Features of the Role:• Opportunity to work in a reputed state university• Hands-on research exposure in pharmaceutical sciences• Participation in project implementation and reporting• Scope for academic publications and research presentations• Strong foundation for Ph.D. or senior research roles• Collaborative academic research environmentResponsibilities• Assist in planning and execution of research project activities• Conduct laboratory experiments and analytical studies• Collect, compile, and interpret research data• Maintain proper laboratory and research documentation• Prepare periodic progress reports• Support manuscript drafting and research publications• Ensure compliance with research ethics and safety guidelines• Coordinate with faculty members and research team• Participate in meetings and project review discussionsRequired Qualifications• M. Pharm from a recognized universityEducational Requirements:Master of Pharmacy (M. Pharm) in a relevant specialization such as Pharmaceutics, Pharmacology, Pharmaceutical Chemistry, or related field. Academic background should align with the project requirements.Experience and Skills:Technical Skills:• Strong knowledge of pharmaceutical research methodologies• Laboratory handling and analytical techniques• Data analysis and interpretation• Understanding of research documentation standardsCore Competencies:• Analytical thinking and problem-solving ability• Good written and verbal communication skills• Ability to work independently and in a research team• Attention to detail and accuracy• Time management and project coordination skillsAge Eligibility:• Minimum Age: 21 Years• Maximum Age: 45 Years• Age relaxation applicable as per organization normsSalary Insights:Remuneration will be provided as per project funding guidelines and university norms. Salary structure will depend on the funding agency and institutional policies.Important Dates:• Starting Date of Application: 27-02-2026• Closing Date of Application: 10-03-2026Organization OverviewJadavpur University is a prestigious public state university located in Kolkata, known for excellence in engineering, science, arts, and interdisciplinary research. The university has a strong research culture and actively engages in funded projects across various scientific domains.Working at Jadavpur University provides exposure to academic excellence, collaborative research, and innovation-driven projects.FAQsQ1: Is this a permanent position?No, this is a project-based contractual position.Q2: Is prior research experience required?While not always mandatory, candidates with research exposure may have an advantage.Q3: Can fresh M. Pharm graduates apply?Yes, if they meet the eligibility criteria specified in the official notification.Q4: Is there age relaxation?Yes, age relaxation is applicable as per organization norms.Q5: What are future career prospects?Candidates may pursue Ph.D., Research Associate roles, or industry R&D opportunities after this role.Application Tips• Highlight M. Pharm specialization clearly• Mention thesis work and research projects• Include laboratory and analytical skills• Attach updated CV with academic achievements• Apply before 10-03-2026Official Notification Click Here

Why This Role MattersCancer survivorship care requires innovative, accessible, and patient-centered follow-up systems. This project focuses on implementing and assessing a tele-consultation program designed for local need-based cancer survivorship care.As a Senior Project Assistant at Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), you will directly contribute to improving cancer follow-up services, enhancing patient engagement, and reducing barriers to telemedicine access.This is an opportunity to work in an ICMR-funded oncology research project that combines community outreach, clinical research, patient counseling, and tele-health innovation.Job DescriptionApplications are invited from eligible candidates to work on a contract basis in an externally funded research project at JIPMER, Puducherry.The Senior Project Assistant will support implementation and evaluation of a tele-consultation program for cancer survivorship care. The role involves patient counseling, tele-follow-up coordination, community engagement, data collection, and research documentation.The candidate will work closely with the Principal Investigator and the oncology department team to ensure smooth execution of project activities.Key Features of the Role:• ICMR-funded oncology research project• Direct patient interaction and tele-follow-up involvement• Community-level outreach exposure• Research documentation and data management experience• Fixed monthly remuneration• Strong foundation for careers in clinical research and oncologyResponsibilities• Conduct patient counseling for tele-consultation and follow-up• Identify barriers to tele-follow-up services• Assist in remote follow-up calls• Prepare Standard Operating Procedures (SOPs) for community engagement• Coordinate with community health workers and general practitioners• Support community outreach and data collection• Maintain research records and documentation• Assist in administrative tasks related to project functioning• Participate in all study-related activities assigned by the PI• Ensure compliance with research ethics and clinical standardsRequired QualificationsEssential:• Bachelor’s degree (3 years) in Social Work / Sociology / Pharmacology / Life Sciences / Nursing / related discipline with two years of relevant experienceOR• Postgraduate degree in Social Work / Sociology / Pharmacology / Life Sciences / Nursing / related disciplineAND• Minimum one year of clinical research experience in Oncology / Psycho-oncology / Community Health / Tele-follow-up / related health research areaEducational Requirements:Candidates with B. Pharm, M. Pharm, B.Sc Nursing, or M.Sc Nursing may apply if they meet the essential criteria and clinical research experience requirements.Experience and Skills:Desirable Skills:• Experience in patient and caregiver counseling• Knowledge of Good Clinical Practice (GCP) guidelines• Experience in clinical research data collection and management• Basic understanding of research methodology• Proficiency in local language (speaking, reading, writing)• Basic computer skills (MS Office, Excel, Word, Video Conferencing tools)• Strong communication and coordination skillsAge Eligibility:• Minimum Age: 21 Years• Maximum Age: 35 Years• Maximum age limit up to 35 years as on last date of receipt of applications• Age relaxation applicable as per organization normsSalary Insights:• Consolidated Remuneration: ₹30,600/- per month (Fixed)• Duration: 1 Year 3 Months (Contract Basis)Important Dates:• Starting Date of Application: 16-02-2026• Closing Date of Application: 08-03-2026Organization OverviewJawaharlal Institute of Postgraduate Medical Education and Research (JIPMER) is a premier medical institute under the Government of India, known for excellence in medical education, research, and patient care.The project is funded by the Indian Council of Medical Research (ICMR), India’s apex biomedical research body supporting innovative healthcare research initiatives.FAQsQ1: Is this a permanent position?No, this is a contract-based position for 1 year and 3 months.Q2: Is clinical research experience mandatory?Yes, minimum one year of relevant clinical research experience is essential.Q3: Is oncology experience preferred?Yes, oncology or related health research experience is preferred.Q4: What is the salary?₹30,600/- per month (fixed).Q5: Is local language proficiency required?It is desirable, especially for community-level coordination and outreach.Application Tips• Clearly mention clinical research experience in your CV• Highlight oncology or tele-follow-up experience• Include GCP training certification if available• Emphasize counseling and communication skills• Apply before 08-03-2026Official Notification and Application Form Click Here

Why This Role MattersResearch institutions play a crucial role in advancing scientific knowledge and technological innovation. A Junior Research Fellow (JRF) contributes directly to academic research projects, experimental studies, and data-driven discoveries that influence future scientific and industrial developments.At Indian Institute of Engineering Science and Technology Shibpur (IIEST Shibpur), this role offers young professionals an opportunity to work closely with faculty members on sponsored research projects, develop strong analytical skills, and gain hands-on experience in applied research environments.For candidates planning to pursue higher studies (Ph.D.) or long-term careers in research, academia, pharmaceuticals, biotechnology, or engineering innovation, this position serves as a strong foundation.Job DescriptionThe Junior Research Fellow (JRF) will assist in executing ongoing research projects under the supervision of the Principal Investigator (PI). The role includes conducting literature reviews, performing laboratory or technical work (as applicable to the project), collecting and analyzing data, maintaining research documentation, and preparing reports.The candidate will also support project documentation, assist in manuscript preparation, and contribute to presentations or publications arising from the research work. Depending on the project’s scope, the JRF may work in laboratory settings, field studies, computational research, or interdisciplinary environments.Key Features of the Role:• Opportunity to work in a reputed technical institution• Hands-on research experience under experienced faculty• Exposure to academic publications and project documentation• Development of analytical, technical, and research skills• Strong foundation for Ph.D. or higher research roles• Collaborative academic environmentResponsibilities• Assist in execution of assigned research project tasks• Conduct literature surveys and background research• Perform laboratory experiments / technical analyses (as per project requirement)• Collect, compile, and analyze research data• Maintain proper research records and documentation• Prepare progress reports and presentations• Support preparation of manuscripts for publication• Ensure compliance with institutional research guidelines• Coordinate with research team members and facultyRequired QualificationsCandidates must possess any of the following qualifications:• MBBS• B.E. / B.Tech• B.Pharm• B.Sc• M.ScEducational Requirements:A recognized degree in Medicine, Engineering, Pharmacy, or Science disciplines. Preference may be given to candidates with strong academic performance and research aptitude.Experience and Skills:Technical Skills:• Basic understanding of research methodology• Knowledge relevant to the specific project domain• Data analysis and documentation capability• Familiarity with laboratory or technical equipment (if applicable)Core Competencies:• Strong analytical and problem-solving skills• Good written and verbal communication skills• Ability to work independently and within a research team• Attention to detail and documentation accuracy• Willingness to learn and adaptAge Eligibility:• Minimum Age: 21 Years• Maximum Age: 45 Years(Age relaxation, if applicable, as per institute norms.)Salary Insights:Remuneration will be as per institutional and project guidelines applicable for Junior Research Fellow positions. Salary structure and tenure will depend on funding agency norms and project duration.Important Dates:• Starting Date for Application: 28-02-2026• Closing Date for Application: 09-03-2026Company OverviewIndian Institute of Engineering Science and Technology Shibpur (IIEST Shibpur) is a premier public technical university located in West Bengal, India. The institute is known for its strong academic programs in engineering, science, and technology, along with its emphasis on research and innovation.With a legacy of academic excellence, IIEST Shibpur provides a vibrant research ecosystem that encourages interdisciplinary collaboration, critical thinking, and innovation-driven development.FAQsQ1: Is prior research experience mandatory?Not mandatory, but candidates with research exposure will have an advantage.Q2: Is this a permanent position?No, JRF positions are typically project-based and temporary in nature.Q3: Can candidates from multiple disciplines apply?Yes, as long as the qualification matches the project requirement.Q4: Is there an age relaxation policy?Age relaxation may apply as per institute or funding agency norms.Q5: What are the career prospects after JRF?Candidates may pursue Ph.D., research associate roles, academic positions, or industry R&D careers.Application Tips• Highlight relevant academic and project experience• Mention research internships or laboratory exposure• Emphasize analytical and technical skills• Attach updated CV with academic achievements• Apply before the closing date (09-03-2026)Official Notification and Application Link Click Here

Why This Role MattersPharmacists are the backbone of safe and effective medication management. In government healthcare systems like the Ex-Servicemen Contributory Health Scheme (ECHS), pharmacists play a vital role in serving ex-servicemen and their dependents by ensuring accurate dispensing, patient counselling, and compliance with medical prescriptions.This role is not limited to dispensing medicines—it directly supports patient safety, therapeutic outcomes, and responsible drug usage. Working within ECHS allows professionals to contribute to the well-being of defense veterans and their families while gaining valuable experience in structured healthcare environments.Job DescriptionThe Pharmacist will be responsible for dispensing prescribed medications, maintaining pharmacy records, managing inventory, and ensuring compliance with applicable pharmaceutical regulations.The role includes verifying prescriptions, checking drug interactions, counselling patients on dosage and precautions, and maintaining proper documentation. The selected candidate will coordinate with medical officers and nursing staff to ensure timely availability of medicines and adherence to treatment protocols.The position requires strong attention to detail, ethical responsibility, and patient-focused communication skills.Key Features of the Role:• Government healthcare setup exposure• Direct patient interaction and counselling• Responsibility for medication safety and compliance• Structured pharmacy inventory management• Opportunity to serve ex-servicemen communityResponsibilities• Dispense medicines as per valid prescriptions• Verify dosage, frequency, and potential drug interactions• Maintain proper pharmacy records and documentation• Manage stock, storage, and inventory control• Ensure medicines are stored as per recommended conditions• Maintain compliance with pharmacy regulations and guidelines• Provide patient counselling regarding medication usage and precautions• Coordinate with medical officers for clarification of prescriptions• Ensure proper labeling and packaging of medicines• Monitor expiry dates and manage disposal of expired stockRequired Qualifications• B.Pharm from a recognized institution• Valid Pharmacy Council registration (if applicable as per norms)Educational Requirements:Bachelor of Pharmacy (B.Pharm) from a recognized university or institution. Candidates must meet eligibility criteria as per ECHS recruitment guidelines.Experience and Skills:Technical Competencies:• Strong knowledge of pharmacology and drug interactions• Understanding of prescription verification processes• Familiarity with inventory and stock management• Knowledge of pharmaceutical regulationsCore Skills:• Attention to detail• Patient counselling and communication skills• Ethical and professional conduct• Organizational and record-keeping ability• Ability to work in a structured healthcare environmentSalary Insights:Remuneration will be provided as per ECHS guidelines and government-approved salary structures. The compensation may vary depending on experience and policy norms.Important Dates:• Last Date of Application: 05-03-2026Organization OverviewEx-Servicemen Contributory Health Scheme (ECHS) is a Government of India healthcare initiative designed to provide medical care to ex-servicemen and their dependents. The scheme operates through a network of polyclinics, service hospitals, and empanelled healthcare providers across the country.ECHS ensures quality healthcare access to veterans while maintaining structured medical and pharmaceutical service standards.FAQsQ1: Is prior experience mandatory?Experience may be preferred but eligibility will depend on official notification norms.Q2: Is registration with Pharmacy Council required?Yes, valid registration is generally required as per pharmacy practice regulations.Q3: Is this a permanent government job?The nature of appointment (contractual/permanent) will depend on official ECHS notification details.Q4: Does the role involve patient interaction?Yes, patient counselling and interaction are key responsibilities.Q5: Where will the posting be?Posting location depends on ECHS polyclinic allocation and recruitment notice.Application Tips• Ensure B.Pharm qualification is clearly mentioned• Attach valid registration certificate (if required)• Highlight dispensing and inventory management experience• Submit application before 05-03-2026• Follow official notification guidelines carefullyOfficial Notification Click Here

Why This Role MattersPharmacists play a crucial role in ensuring the safe preparation, dispensing, and management of medicines in public healthcare systems. Under the National Ayush Mission Kerala (NAM Kerala), pharmacists contribute to strengthening AYUSH healthcare services across the state.This role supports the distribution of traditional and modern medicinal systems under regulated conditions, ensuring patient safety and adherence to healthcare standards. Working with NAM Kerala allows candidates to contribute directly to public health services while gaining valuable government healthcare experience.Job DescriptionThe Pharmacist will be responsible for dispensing prescribed medicines, maintaining pharmacy stock, and ensuring proper documentation within the assigned healthcare unit under NAM Kerala.The selected candidate must verify prescriptions, maintain inventory records, monitor stock levels, and ensure medicines are stored according to recommended guidelines. The role also involves coordinating with medical officers and healthcare staff to ensure uninterrupted medicine availability.This is a patient-focused and compliance-driven position requiring accuracy, ethical conduct, and strong organizational skills.Key Features of the Role:• Government healthcare exposure under AYUSH mission• Structured pharmacy management responsibilities• Fixed monthly remuneration• Public health service contribution• Opportunity to work within Kerala healthcare frameworkResponsibilities• Dispense medicines as per valid prescriptions• Maintain stock registers and inventory records• Monitor expiry dates and ensure proper storage conditions• Maintain proper documentation of drug distribution• Ensure compliance with pharmacy guidelines and healthcare policies• Assist medical officers in medicine procurement planning• Handle patient queries regarding dosage and precautions• Maintain cleanliness and organization of pharmacy unit• Support reporting and audit requirementsRequired Qualifications• D.Pharm (Diploma in Pharmacy) from a recognized institution• Registration with the State Pharmacy Council (as applicable)Educational Requirements:Diploma in Pharmacy (D.Pharm) from a recognized board or university. Candidates must meet eligibility criteria as prescribed by NAM Kerala.Experience and Skills:Technical Knowledge:• Basic pharmacology knowledge• Understanding of prescription verification• Inventory and stock management skills• Knowledge of medicine storage requirementsCore Competencies:• Attention to detail• Good communication skills• Record-keeping ability• Ethical and professional conduct• Ability to work in government healthcare settingsAge Eligibility:• Minimum Age: 18 Years• Maximum Age: 40 Years• Age should not exceed 40 years as on the date of interview• Age relaxation applicable as per organization normsSalary Insights:• Monthly Remuneration: ₹14,700/-Compensation is fixed as per NAM Kerala norms and applicable government guidelines.Important Date:• Closing Date of Application: 05-03-2026Organization OverviewNational Ayush Mission Kerala (NAM Kerala) operates under the Ministry of AYUSH, Government of India, with the objective of promoting and strengthening AYUSH healthcare services including Ayurveda, Yoga, Unani, Siddha, and Homeopathy across the state.The mission focuses on accessible, affordable, and quality traditional healthcare services through government-supported facilities and programs.FAQsQ1: Is this a permanent government job?The appointment is generally contractual as per mission norms.Q2: Is D.Pharm mandatory?Yes, D.Pharm is the required qualification for this post.Q3: Is registration required?Yes, valid State Pharmacy Council registration is typically required.Q4: What is the age calculation date?Age must not exceed 40 years as on the date of interview.Q5: What is the salary structure?The fixed monthly remuneration is ₹14,700/- as per mission guidelines.Application Tips• Ensure D.Pharm qualification and registration details are clearly mentioned• Attach relevant certificates and age proof documents• Submit application before 05-03-2026• Verify eligibility criteria carefully before applying• Keep documents ready for interview verificationOfficial Notification and Application FormClick Here

Why This Role MattersRegulatory and clinical documents are the foundation of global drug development. Every protocol, clinical study report, and regulatory submission submitted to health authorities influences decisions that impact patient access to innovative therapies. High-quality medical writing ensures clarity, scientific integrity, regulatory compliance, and timely approvals.At Thermo Fisher Scientific, through its clinical research division PPD, the FSP Medical Writer plays a critical role in supporting global clients within a Functional Service Partnership model. This role ensures that complex clinical data is transformed into clear, compliant, and submission-ready regulatory documentation.If you are scientifically strong, detail-oriented, and confident in regulatory writing, this position provides exposure to global regulatory standards and structured content authoring systems while supporting life-changing therapies worldwide.Job DescriptionThe FSP Medical Writer is responsible for developing, editing, and finalizing high-quality clinical and regulatory documents dedicated to one or more clients within the FSP model. The role involves authoring Clinical Study Reports (CSRs), protocols, Investigator’s Brochures (IBs), regulatory submissions, and other essential clinical documentation.The position requires collaboration with cross-functional teams including clinical operations, biostatistics, regulatory affairs, safety, and project management to ensure scientific accuracy and regulatory compliance. The writer must ensure that documents align with ICH, FDA, and other international regulatory standards while meeting internal quality benchmarks and client expectations.Experience in structured content authoring systems, automation tools, and AI-supported content workflows is advantageous, as the organization continues to enhance digital medical writing capabilities.Key Features of the Role:• Client-dedicated position within the FSP model• Exposure to global regulatory submissions• Opportunity to work with structured content authoring systems• Involvement in AI-driven content creation and automation initiatives• Strong pathway into senior medical writing or regulatory leadership roles• Cross-functional collaboration across global clinical development teamsResponsibilitiesMedical & Regulatory Writing:• Write and edit Clinical Study Reports (CSRs)• Develop study protocols and amendments• Author Investigator’s Brochures (IBs)• Prepare regulatory submission documents• Contribute to safety writing such as DSURs (if applicable)Document Quality & Compliance:• Ensure documents align with regulatory guidelines and company standards• Apply ICH, FDA, and global regulatory requirements• Maintain clarity, consistency, and scientific accuracy• Provide structured, submission-ready documentationCollaboration & Review:• Partner with cross-functional teams to gather and verify clinical data• Provide input on document structure and presentation• Review and provide feedback on documents prepared by other writers• Manage timelines and deliverables for assigned projectsDigital & Innovation Support:• Work within structured content management systems• Support AI-driven content creation initiatives• Utilize automation tools to enhance efficiency• Stay updated on evolving medical writing technologies and standardsRequired Qualifications• Bachelor’s degree in a scientific discipline (Advanced degree preferred)• Minimum 2+ years of regulatory medical writing experience• Experience within pharmaceutical or CRO industry requiredEducational Requirements:Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Medicine, or related scientific discipline. A Master’s or advanced scientific degree is preferred for candidates seeking long-term growth in regulatory writing leadership roles.Experience and Skills:Technical Knowledge:• Extensive knowledge of regulatory guidelines and drug development processes• Understanding of GCP and ICH guidelines• Familiarity with FDA and global regulatory agency requirements• Experience writing CSRs, protocols, IBs, and regulatory submissionsPreferred Expertise:• Experience in safety writing (e.g., DSUR)• Experience with structured content management systems• Familiarity with AI-driven content creation and Natural Language Generation toolsProfessional Competencies:• Strong organizational and program management skills• Proven leadership capability to mentor or guide team members• High level of independence in decision-making• Strong analytical thinking and problem-solving skills• Excellent written and verbal communication• Strong interpersonal skills for stakeholder collaboration• Ability to work effectively in cross-cultural, global teamsSalary Insights:Compensation will be competitive and aligned with industry standards for medical writing roles within global CRO environments.Additional benefits may include:• Comprehensive health and wellness benefits• Flexible working culture supporting work-life balance• Award-winning learning and development programs• Exposure to advanced digital medical writing platforms• Long-term career progression opportunitiesCompany OverviewThermo Fisher Scientific is a global leader in scientific services, employing over 100,000 colleagues worldwide. Through its clinical research division PPD, the organization conducts clinical trials in more than 100 countries and supports the development of innovative therapies across therapeutic areas.The company’s mission is to enable customers to make the world healthier, cleaner, and safer. Guided by its core values—Integrity, Intensity, Innovation, and Involvement Thermo Fisher Scientific fosters collaboration, scientific excellence, and technological advancement.Employees benefit from a collaborative global culture with a local feel, structured professional growth programs, and strong support for work-life balance.FAQsQ1: Is this a remote role?The role follows a standard office schedule (Mon–Fri) but may operate within flexible FSP arrangements depending on client needs.Q2: Is safety writing mandatory?Safety writing experience (e.g., DSUR) is advantageous but not mandatory.Q3: Is structured content authoring experience required?Not mandatory, but strongly preferred for candidates interested in digital innovation.Q4: Does the role involve leadership responsibilities?Yes, experienced candidates may mentor junior writers and manage document workflows.Q5: What are the career progression opportunities?Potential growth includes Senior Medical Writer, Lead Medical Writer, Regulatory Writing Manager, or Global Submission Lead roles.Application Tips• Highlight CSR, protocol, and IB writing experience clearly• Mention regulatory submission involvement• Emphasize structured content or AI-tool exposure• Demonstrate ability to manage timelines independently• Showcase collaboration with cross-functional clinical teams

Why This Role MattersIn clinical research and regulatory submissions, accuracy is non-negotiable. Every protocol, clinical study report, investigator brochure, and safety narrative contributes directly to regulatory decisions that impact patient access to life-changing therapies. A single inconsistency in data tables, formatting, or scientific logic can delay approvals and affect global health outcomes.At Thermo Fisher Scientific, through its PPD clinical research portfolio, this role ensures regulatory documents meet the highest quality standards before submission. As a Document Review Specialist II within the Medical Writing Functional Service Partnership (FSP) team, you serve as a critical quality checkpoint for global clinical programs conducted across 100+ countries.This position is ideal for detail-oriented professionals with strong regulatory knowledge who thrive in structured, high-accountability environments and want to contribute to global clinical development excellence.Job DescriptionThe Document Review Specialist II is responsible for reviewing highly technical scientific and regulatory documents to ensure clarity, accuracy, consistency, and compliance with industry standards. Working within the FSP model, you will be dedicated to one or more clients and collaborate closely with medical writers, regulatory teams, and cross-functional stakeholders.You will review documents such as Clinical Study Reports (CSRs), study protocols, amendments, Investigator’s Brochures (IBs), Informed Consent Forms (ICFs), regulatory submissions, and patient safety narratives. The role requires verifying data accuracy across tables, listings, and figures; ensuring alignment with templates and editorial style guides; and confirming adherence to ICH, FDA, and international regulatory standards.This role demands meticulous attention to detail, advanced English proficiency, scientific comprehension, and the ability to manage priority reviews under tight timelines.Key Features of the Role:• Dedicated client-facing role within the FSP model• Exposure to global regulatory documentation standards• Involvement in high-impact clinical research submissions• Opportunity to work in a remote, cross-cultural team environment• Strong pathway into advanced medical writing or regulatory operations roles• Engagement with document management systems and structured workflowsResponsibilitiesDocument Quality Review & Editing:• Review highly technical scientific documents for quality and compliance• Verify scientific logic and clarity of document content• Cross-check data in tables, listings, and figures against source documents• Edit for grammatical correctness, consistency, and formatting accuracy• Ensure compliance with client templates and editorial style guidesRegulatory Compliance & Standards Alignment:• Apply current ICH, FDA, and global regulatory guidelines• Maintain awareness of industry standards and template updates• Ensure document alignment with regulatory expectationsCollaboration & Communication:• Proactively query authors regarding inconsistencies or scientific concerns• Support effective communication between internal teams and clients• Adjust schedules to accommodate urgent or priority review requests• Contribute to operational excellence and timely deliverablesSystem & Process Management:• Work within document management systems• Support template compliance through direct formatting in Microsoft Word• Maintain organized documentation tracking and review workflowsRequired Qualifications• Bachelor’s degree or equivalent academic/vocational qualification• Minimum 2+ years of experience reviewing regulatory documents such as CSRs, Protocols, ICFs, and IBs• Experience within pharmaceutical, biotechnology, or CRO industry preferredEducational Requirements:A Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Biomedical Sciences, English (Scientific Writing), or a related discipline is required. Additional certifications in medical writing or regulatory affairs are advantageous.Experience and Skills:Technical & Regulatory Knowledge:• Strong understanding of medical writing processes• Familiarity with GCP guidelines and ICH standards• Knowledge of FDA and international regulatory requirements• Understanding of statistical concepts used in clinical documentsDocument & Editorial Skills:• Advanced English proficiency (written and verbal)• Strong grammatical and editing capability• Ability to focus on both micro-level details and overall document intent• Experience with direct formatting in Microsoft WordSystems & Digital Skills:• Working knowledge of document management systems• Advanced computer literacy• Comfortable working in digital and decentralized environmentsProfessional Competencies:• Strong analytical thinking• Excellent organizational and planning skills• Ability to work under pressure• Effective team collaboration in cross-cultural settings• Capacity to work independently in remote environmentsSalary Insights:Compensation will be competitive and aligned with industry benchmarks for medical writing and document review roles within global CRO environments.Additional benefits may include:• Comprehensive health and wellness benefits• Flexible working culture supporting work-life balance• Structured learning and development programs• Exposure to global clinical research frameworksCompany OverviewThermo Fisher Scientific is a global leader in scientific services and life sciences solutions, employing over 100,000 colleagues worldwide. Through its clinical research division PPD, the organization conducts clinical trials in more than 100 countries and supports the development of life-changing therapies.The company’s mission is to enable customers to make the world healthier, cleaner, and safer. Its values—Integrity, Intensity, Innovation, and Involvement—guide teams across laboratory services, digital solutions, and decentralized clinical trial operations.Employees benefit from award-winning learning and development programs, a collaborative global culture, and strong support for career growth in regulatory science and clinical research operations.FAQsQ1: Is CRO experience mandatory?Not mandatory, but experience within pharmaceutical or CRO environments is strongly preferred.Q2: Is this a medical writing role?This is a document review and quality assurance role within medical writing, not primary authoring.Q3: Does the role require client interaction?Yes, especially within the FSP model where professionals may support dedicated clients.Q4: Is remote work allowed?Yes, the role is remote-based within a structured office schedule (Mon–Fri).Q5: What career growth opportunities exist?This role can lead to Senior Document Review Specialist, Medical Writer, Regulatory Writing Lead, or Quality Compliance roles within clinical research.Application Tips• Highlight experience reviewing CSRs, Protocols, ICFs, and IBs• Emphasize regulatory guideline familiarity (ICH, FDA, GCP)• Showcase editing, formatting, and template compliance skills• Mention experience with document management systems• Demonstrate ability to manage priority reviews under deadlines

Why This Role MattersIn pharmaceutical manufacturing, quality is not just a function—it is a responsibility that directly impacts patient safety and public health. Every batch released to the market represents trust. Trust that processes were validated, systems were controlled, data was reliable, and compliance standards were met without compromise.At the Goa manufacturing site of Sanofi, the Quality Assurance Specialist plays a central role in maintaining and strengthening the site’s Quality Management System (QMS). From deviation management and change control to validation oversight and batch release support, this role ensures that global standards and regulatory expectations are consistently upheld.This position is ideal for pharmaceutical professionals who are disciplined, compliance-driven, and passionate about maintaining cGMP standards while contributing to continuous improvement initiatives.Job DescriptionThe Quality Assurance Specialist is responsible for managing and overseeing quality systems at the Goa manufacturing site. The role includes end-to-end management of product quality reviews, deviation handling, change control coordination, validation oversight, batch record review, and regulatory compliance activities.The position acts as a QA focal point for multiple systems including OOS/OOT management, CAPA, training systems, market complaint investigations, validation programs, and global standard implementation.The selected candidate will work cross-functionally with Production, Engineering, QC, PMTD, HSE, and global stakeholders to ensure that all manufacturing and quality operations align with cGMP requirements and global company standards.Key Features of the Role:• End-to-end exposure to pharmaceutical Quality Management Systems• Direct involvement in validation, qualification, and compliance oversight• Responsibility for deviation, CAPA, and change control systems• Active role in batch record review and release support• Interaction with global standards (STDs & GOPs) implementation• Opportunity to contribute to data integrity and digital compliance initiatives• Involvement in audit readiness and regulatory inspection preparednessResponsibilities1. Management of Quality Systems• Compilation, review, and management of Product Quality Reviews (PQR)• Act as site coordinator for change control management• Manage deviation systems and support investigations• Oversee Market Complaint investigations• Act as QA focal point for OOS/OOT management• Manage training systems and cGMP training coordination• Oversight of Pest Control systems• Perform Nitrosamine assessments and ICH Q3D compliance reviews• Implement Sanofi Global Standards (STDs) and Global Operating Procedures (GOPs)• Manage subcontractor and service provider quality compliance• Oversee validation systems (process, cleaning, transport, computerized systems)• Manage CAPA systems and ensure timely closure2. Quality Management Systems (QMS)• Coordinate and conduct self-inspections as per annual planner• Review and approve GxP documents, BMRs, and BPRs in electronic systems• Manage SOPs, master documents, and document control systems• Initiate and close change controls and deviations• Support market complaint investigations• Implement and monitor assigned CAPAs and Efficiency Reviews (ERs)• Act as PPO for assigned Quality Maturity Index (QMI) processes• Support batch release and respond to QP queries• Manage data integrity aspects and audit trail reviews• Participate in SMS and HSE initiatives• Maintain Site Master File (SMF)• Review calibration documentation (Engineering/QC/PMTD)• Manage user access control and document archival systems• Support analytical method creation3. Validation & Qualification Oversight• Act as quality focal point for all validation activities– Process validation– Cleaning validation– Transport validation– Computerized system validation• Oversee temperature and relative humidity mapping• Monitor hold time studies (products and equipment)• Provide QA oversight for utilities and purified water systems• Manage Site Qualification & Validation Master Plan4. In-Process Quality Assurance (IPQA)• Review and approve Master Batch Records and executed Batch Records• Review and approve production logbooks• Perform line clearance in production areas• Conduct in-process quality checks• Perform sampling during routine production and validation• Provide shopfloor QA oversight5. Health, Safety & Environment (HSE)• Ensure adherence to all HSE policies and procedures• Promote safe working conditions and continuous safety improvement• Conduct daily training in +QDCI meetings to address unsafe conditions• Encourage associate suggestions for safety improvements• Review and evaluate implemented safety procedures• Train personnel to ensure zero LTI and IWLT at the workplaceRequired Qualifications• B.Pharm or M.Pharm• 2–5 years of experience in pharmaceutical Quality AssuranceEducational Requirements:Bachelor’s or Master’s degree in Pharmacy from a recognized institution. Strong understanding of cGMP, regulatory guidelines, and pharmaceutical manufacturing practices is essential.Experience and Skills:Technical Competencies:• Strong knowledge of cGMP requirements• Experience in deviation, CAPA, and change control management• Validation and qualification oversight experience• Experience with electronic document management systems• Understanding of data integrity principles• Familiarity with regulatory guidelines (ICH, global GMP standards)Core Skills:• Strong analytical and problem-solving abilities• Attention to detail and documentation accuracy• Cross-functional coordination skills• Audit readiness mindset• Strong written and verbal communication skillsSalary Insights:Compensation will be competitive and aligned with pharmaceutical industry standards. It will depend on experience, expertise in quality systems, and interview performance.Additional benefits may include:• Exposure to global quality systems• Structured career growth within a multinational pharmaceutical environment• Learning opportunities aligned with international regulatory standardsCompany OverviewSanofi is a global biopharmaceutical company focused on human health. The organization develops vaccines, innovative treatments, and solutions for rare diseases and chronic conditions. With operations across multiple countries, Sanofi integrates science, technology, and global expertise to deliver transformative healthcare solutions.The company is committed to diversity, equity, and inclusion, ensuring equal opportunity regardless of race, religion, gender, nationality, disability, or identity. Sanofi fosters a culture where professionals from diverse backgrounds collaborate to drive scientific excellence and meaningful patient impact.FAQsQ1: Is prior QA experience mandatory?Yes, 2–5 years of pharmaceutical QA experience is required.Q2: Does the role involve shopfloor activities?Yes, IPQA responsibilities include line clearance, in-process checks, and production oversight.Q3: Is validation experience necessary?Yes, oversight of validation and qualification systems is a key responsibility.Q4: Does this role support batch release?Yes, it includes review support and response to QP queries.Q5: Are multilingual skills preferred?Yes, knowledge of English, Hindi, Konkani, or Marathi is advantageous.Application Tips• Highlight deviation, CAPA, and change control experience clearly• Mention validation and qualification exposure• Emphasize shopfloor IPQA experience• Demonstrate understanding of data integrity principles• Showcase audit preparation or regulatory inspection involvement

Why This Role MattersIn a highly regulated global trade environment, ensuring compliance with export controls, embargo laws, and product restrictions is critical to maintaining operational integrity and protecting organizational reputation. Every international shipment must meet strict regulatory requirements before crossing borders. Even minor documentation gaps or screening errors can result in shipment delays, financial penalties, or legal consequences.This role serves as a vital checkpoint within the supply chain, ensuring that customers, products, and transactions comply with European trade regulations. By conducting structured order screening, verifying regulatory documentation, and collaborating across departments, you help safeguard lawful and seamless cross-border operations.Beyond operational efficiency, this position directly contributes to risk mitigation and governance excellence. It provides early-career professionals an opportunity to build expertise in export control, regulatory compliance, ERP systems, and digital workflow management—skills that are increasingly valuable in global supply chain leadership roles.Job DescriptionThe Export Control & Order Screening Specialist is responsible for ensuring compliant and timely order processing by screening customers, products, and shipments against European regulatory requirements. This includes restricted party screening, embargo verification, export control flag checks, and documentation validation.The role requires close coordination with external customers, supply chain teams, logistics partners, trade compliance functions, and customer service departments to prevent the shipment of restricted items and resolve compliance-related order blocks.The selected candidate will perform end-to-end order screening, communicate documentation requirements, track document submissions, and ensure that regulatory approvals are secured prior to shipment release. The position demands strong attention to detail, regulatory awareness, documentation discipline, and the ability to interpret and apply compliance rules accurately.In addition to operational tasks, the role involves supporting continuous improvements in screening processes and digital documentation workflows.Key Features of the Role:• Exposure to European trade compliance and export control frameworks• Direct involvement in restricted party and embargo screening• Hands-on experience with ERP systems such as SAP• Cross-functional collaboration with Sales, Logistics, and Trade Compliance teams• Participation in digital transformation and process optimization initiatives• Structured pathway into advanced global trade governance rolesResponsibilitiesOrder Screening & Risk Assessment:• Conduct restricted party screening for customers and stakeholders• Perform embargo checks and export control flag evaluations• Screen regulated products to ensure compliance with European regulations• Identify compliance risks and determine appropriate action• Release or block orders in ERP systems based on regulatory assessmentDocumentation Verification & Customer Coordination:• Communicate documentation requirements such as EUDs, permits, declarations, and licenses• Send timely follow-ups and reminders to secure required documents• Review and validate submitted documents for completeness and accuracy• Archive compliance documentation in accordance with global standardsCross-Functional Collaboration:• Work closely with Sales, Supply Chain, Logistics, Trade Compliance, and Customer Service teams• Resolve order blocks efficiently to minimize shipment delays• Support supply chain prioritization once compliance readiness is confirmedProcess & Digital Enhancement:• Maintain understanding of product classification and shipping workflows• Contribute to continuous improvement in screening and documentation processes• Support digital enablement initiatives to enhance compliance efficiency• Assist with exception monitoring and workflow optimizationRequired Qualifications• Postgraduate degree in Life Sciences (Chemistry, Biochemistry, Biotechnology, Microbiology)OR• Graduate/Postgraduate degree in Supply Chain, Logistics, International Business, or related fields• 1–2 years of relevant experience in Order Management, Supply Chain Operations, Trade Compliance, Logistics Coordination, or Scientific IndustryEducational Requirements:Candidates must possess a graduate or postgraduate qualification in Life Sciences, Supply Chain, Logistics, International Business, or related disciplines. A postgraduate degree is advantageous for candidates aiming to build a long-term career in trade compliance and global operations governance.Experience and Skills:Technical Knowledge:• Basic to intermediate understanding of regulated product handling in supply chains• Familiarity with export controls, embargoes, and product restrictions• Experience working with SAP or similar ERP systems• Ability to navigate order management, delivery, and customer master screensDigital & Analytical Skills:• Proficiency in Microsoft Office 365 (Excel, Outlook, SharePoint, Teams)• Basic project management capability• Ability to interpret regulatory frameworks and apply them to real-world transactionsPreferred Skills:• Experience using Power BI for dashboards and reporting• Familiarity with AI-based productivity tools such as Microsoft Copilot• Exposure to data analysis, process automation, or digital workflow optimization• Comfort working with online documentation portals and digital compliance systemsCore Competencies:• Strong analytical and decision-making ability• High attention to detail and documentation accuracy• Effective communication skills• Ability to manage multiple tasks under structured regulatory guidelines• Professional and proactive work approachSalary Insights:Compensation will be aligned with industry standards and determined based on qualifications, experience, and interview performance.Additional benefits may include:• Exposure to international trade compliance systems• ERP and digital workflow expertise• Participation in automation and process improvement initiatives• Career growth into senior compliance or global trade rolesCompany OverviewThe organization operates at the intersection of science, technology, and global supply chain excellence. With a strong commitment to innovation and regulatory integrity, it supports the compliant movement of regulated products across international markets.Diversity and inclusion are central to the company’s culture. Employees come from varied professional and academic backgrounds, contributing unique perspectives that drive excellence and continuous improvement. The organization fosters professional growth, encourages curiosity, and empowers employees to build meaningful careers within global operations and compliance functions.By joining this team, you become part of an environment that values accountability, innovation, and inclusive collaboration while contributing to compliant global trade operations that impact industries worldwide.FAQsQ1: Is prior trade compliance experience mandatory?While not mandatory, familiarity with export control regulations is strongly preferred.Q2: Is ERP experience required?Experience with SAP or similar ERP systems is highly desirable.Q3: Does this role involve customer interaction?Yes. The role requires communication with customers to secure and validate regulatory documentation.Q4: Is this a technical or operational role?It combines operational order management responsibilities with regulatory compliance oversight.Q5: What career growth opportunities exist?The role provides progression into senior export control, global trade compliance, or supply chain governance positions.Application Tips• Clearly highlight ERP/SAP experience in your resume• Mention exposure to export control or regulated product environments• Demonstrate attention to detail and compliance discipline• Showcase cross-functional collaboration experience• Emphasize digital tool proficiency and process improvement contributions

Why This Role MattersClinical research is the backbone of medical innovation. From early-stage studies to post-marketing surveillance, well-coordinated site-level operations are essential to maintaining data integrity, patient safety, and regulatory compliance.For over two decades, ProPharma has supported biotech, medical device, and pharmaceutical companies in navigating complex regulatory pathways and accelerating therapeutic development. The Research Assistant role plays a direct part in this mission by ensuring smooth execution of hospital-based clinical studies.This position is ideal for candidates who want hands-on exposure to clinical trial operations within a healthcare environment. By managing site communications, maintaining documentation, and supporting data management processes, the Research Assistant helps ensure that research activities meet IRB and FDA standards while maintaining operational efficiency.Job DescriptionProPharma is hiring a Research Assistant for a hospital-based, on-site role in Nagpur, Maharashtra. This part-time opportunity requires 24 hours per week and involves supporting day-to-day clinical research activities at the site level.The selected candidate will serve as a central coordination point for communication, document management, and study-related administrative processes. Responsibilities include assisting with pre-screening, performing accurate data entry, responding to system queries, monitoring clinical databases, and supporting study closeout activities.This role requires strong organizational discipline, regulatory awareness, attention to detail, and the ability to work both independently and collaboratively within a structured research environment.Key Features of the Role:• Hospital-based clinical research exposure• On-site position in Nagpur, Maharashtra• Part-time schedule (24 hours per week)• 1-year contractual role with possible extension• Direct involvement in IRB/FDA-compliant documentation• Exposure to study team coordination and database monitoring• Opportunity to gain practical clinical research experienceResponsibilitiesClinical Site Communication & Coordination:• Serve as point of contact for daily site communications• Coordinate document submissions and activity timelines• Establish and maintain timely communication with assigned stakeholdersStudy Operations Support:• Assist with patient pre-screening as assigned• Perform accurate data entry into clinical research systems• Evaluate and respond to system-generated queries• Monitor clinical databases to ensure data completeness and accuracy• Support study closeout activitiesRegulatory Compliance & Documentation:• Maintain study documentation in compliance with IRB and FDA policies• Ensure proper filing, tracking, and version control of essential documents• Support audit readiness and regulatory inspectionsGeneral Duties:• Assist the site with additional study-related activities as directed• Perform other duties as assigned to support research objectivesRequired Qualifications• Bachelor’s Degree OR• Equivalent experience defined as a minimum of 3 years of related experienceEducational Requirements:A Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, or related healthcare fields is preferred. Candidates with at least three years of relevant experience in clinical or healthcare settings may also qualify.Experience and Skills:Experience:• Prior study team experience is ideal• Exposure to clinical research environments is advantageousTechnical Skills:• Ability to manage web-based research platforms on Microsoft OS systems• Familiarity with electronic data capture (EDC) systems and clinical databases preferred• Proficiency in data entry and system query managementCore Competencies:• Strong verbal and written communication skills• Critical thinking and analytical abilities• Excellent organizational and multitasking skills• Ability to work independently and collaboratively• Professional and articulate communication style• Initiative-driven while adhering to structured directives• Ability to maintain confidentiality and privacy in working environmentsSalary Insights:Compensation will be aligned with industry standards and will depend on experience, skills, and interview performance.Additional benefits may include:• Exposure to hospital-based clinical research operations• Experience with regulatory-compliant documentation systems• Opportunity for contract extension based on performance• Professional growth within a global consulting environmentCompany OverviewProPharma partners with biotech, medical device, and pharmaceutical organizations across the entire product lifecycle through its advise-build-operate model. With expertise spanning regulatory sciences, clinical research solutions, pharmacovigilance, quality & compliance, medical information, and R&D technology, ProPharma delivers customizable consulting services that accelerate high-impact drug and device programs.The company promotes diversity, equity, and inclusion, fostering a workplace where employees can contribute authentically and grow professionally. All applications are personally reviewed by a recruitment team member, and every candidate receives an application outcome notification.While remote work is supported in general, this specific role is hospital-based and requires on-site presence. All candidates are assessed based on merit without bias related to location proximity.FAQsQ1: Is this role remote?No. This is an on-site hospital-based role in Nagpur, Maharashtra.Q2: Is the position full-time?No. It is a part-time role requiring 24 hours per week.Q3: What is the contract duration?The initial contract is for 1 year, with potential extension based on performance and study requirements.Q4: Is clinical research experience mandatory?While not strictly mandatory, study team experience is strongly preferred.Q5: Does ProPharma use AI screening tools?No. All applications are personally reviewed by a recruitment team member.Application Tip• Highlight any clinical research, hospital, or documentation-handling experience• Mention familiarity with IRB/FDA guidelines if applicable• Emphasize data accuracy and database management skills• Showcase strong communication and coordination abilities• Demonstrate ability to work independently in a structured clinical setting

Why This Role MattersClinical research forms the foundation of modern medical advancement. From early-phase clinical trials to post-marketing studies, structured site operations and accurate documentation are essential to maintaining patient safety, regulatory compliance, and data integrity. Without efficient site-level coordination, even the most promising therapies can face delays or compliance challenges.For more than 20 years, ProPharma has partnered with biotech, medical device, and pharmaceutical organizations to navigate regulatory complexities and accelerate therapeutic innovation. The Research Assistant plays a critical role in this mission by supporting hospital-based clinical trial operations and ensuring seamless coordination between stakeholders.This role is ideal for candidates seeking hands-on experience in real-world clinical research settings. By managing documentation, assisting with data systems, and supporting study coordination, the Research Assistant directly contributes to the quality and success of ongoing research programs.Job DescriptionProPharma is seeking a Research Assistant for a hospital-based role in Nagpur, Maharashtra. This is an on-site, part-time position requiring 24 hours per week. The selected candidate will assist with day-to-day clinical research activities, ensuring regulatory compliance and operational efficiency at the study site.The Research Assistant will serve as a central coordination point for communication, document submissions, database monitoring, and administrative study support. This role requires a disciplined, detail-oriented professional who can manage multiple responsibilities while maintaining compliance with IRB and FDA policies.Strong organizational ability, attention to detail, and the capacity to work independently while collaborating with research teams are essential for success in this position.Key Features of the Role:• Hospital-based clinical research environment• On-site position in Nagpur, Maharashtra• Part-time schedule (24 hours per week)• 1-year contract with potential extension• Direct involvement in IRB/FDA-compliant documentation processes• Exposure to database monitoring and study coordination• Opportunity to build practical experience in clinical research operationsResponsibilitiesClinical Site Communication & Coordination:• Serve as the primary point of contact for daily site communications• Coordinate document submissions and study activity timelines• Establish and maintain consistent communication with assigned stakeholdersStudy Operations Support:• Support patient pre-screening activities as assigned• Perform accurate data entry into research systems• Evaluate and respond to system-generated queries• Monitor clinical databases to ensure accuracy and completeness• Assist with study closeout proceduresRegulatory Compliance & Documentation:• Maintain documentation in compliance with IRB and FDA policies• Ensure proper filing, version control, and document tracking• Support audit preparedness and regulatory inspectionsGeneral Duties:• Assist with additional study-related activities as directed• Perform other assigned tasks to support research objectivesRequired Qualifications• Bachelor’s Degree in Pharmacy• Equivalent experience defined as a minimum of 3 years of related professional experienceEducational Requirements:A Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, or related healthcare disciplines is preferred. Candidates with a minimum of three years of relevant experience in clinical research or healthcare operations may also be considered.Experience and Skills:Experience:• Study team experience is highly desirable• Prior exposure to clinical research settings is advantageousTechnical Skills:• Ability to manage web-based research platforms using Microsoft OS systems• Familiarity with electronic data capture (EDC) systems preferred• Strong data entry accuracy and query management capabilityCore Competencies:• Excellent verbal and written communication skills• Strong analytical and critical thinking ability• Highly organized with effective multitasking skills• Ability to work independently and within collaborative teams• Professional, articulate, and well-spoken• Proactive mindset while following structured directives• Strong commitment to confidentiality and privacy complianceSalary Insights:Compensation will be aligned with industry standards and will depend on qualifications, relevant experience, and interview performance.Additional benefits may include:• Exposure to hospital-based clinical trial operations• Experience working with regulatory-compliant documentation systems• Opportunity for contract extension based on performance• Professional growth within an internationally recognized consulting organizationCompany OverviewProPharma partners with biotech, medical device, and pharmaceutical organizations throughout the complete product lifecycle via its advise-build-operate model. With expertise in regulatory sciences, clinical research solutions, pharmacovigilance, medical information, quality & compliance, and R&D technology, ProPharma delivers fully customizable consulting services that accelerate high-impact drug and device programs.The organization promotes diversity, equity, and inclusion, fostering a workplace where employees can thrive and contribute authentically. All applications are personally reviewed by a recruitment team member, and each candidate receives an outcome notification.Although ProPharma supports remote work in certain roles, this position is hospital-based and requires on-site presence in Nagpur. All candidates are assessed purely on merit without any advantage or disadvantage related to proximity to office locations.FAQsQ1: Is this role remote?No. This is an on-site hospital-based role in Nagpur, Maharashtra.Q2: Is the position full-time?No. It is a part-time role requiring 24 hours per week.Q3: What is the contract duration?The contract is initially for 1 year, with the possibility of extension depending on performance and project needs.Q4: Is prior clinical research experience mandatory?While not mandatory, study team experience is strongly preferred.Q5: How are applications reviewed?All applications are personally reviewed by a recruitment team member; AI screening tools are not used.Application Tip• Highlight relevant clinical research or hospital coordination experience• Mention familiarity with IRB/FDA compliance requirements• Emphasize accuracy in data entry and database monitoring• Showcase communication, organization, and multitasking strengths• Demonstrate ability to maintain confidentiality and regulatory compliance