Kolkata Healthcare Jobs

Why This Role MattersThe Medical Science Liaison (MSL) role at Bayer is pivotal in bridging scientific knowledge and clinical practice. The MSL facilitates the exchange of medical and scientific information with healthcare professionals, supports clinical research, and contributes to the safe and effective use of Bayer products. This role ensures that medical and scientific insights are effectively communicated, fostering evidence-based practice and improving patient outcomes.Job DescriptionBayer is seeking a motivated Medical Science Liaison to join its Pharmaceuticals division in Kolkata, West Bengal, India. This role involves engaging with Thought Leaders, medical societies, and advisory boards, providing scientific support, and participating in educational and training activities within the therapeutic area. The MSL contributes to research dissemination, clinical trial understanding, and strategy implementation.Key Features of the Role• Position: Medical Science Liaison• Organization: Bayer – Pharmaceuticals Division• Location: Kolkata, West Bengal, India• Employment Type: Full-time• Job Reference: 862533Responsibilities• Engage with Thought Leaders (TLs – Doctors) to provide scientific and educational insights• Disseminate, clarify, and educate on scientific data, study protocols, and professional literature• Interact with medical societies and advisory boards, answering scientific queries and organizing meetings• Attend congresses and conventions to network, gather competitive intelligence, and establish professional contacts• Coordinate scientific education events for healthcare professionals within the therapeutic area• Identify, profile, and engage TLs in line with the product Medical Affairs plan• Prepare reports and track activities against agreed objectives• Provide additional external scientific support, training, and education as neededRequired Qualification• Degree in natural sciences or a medical background (MD, MBBS, BAMS, BDS, MDS)Important Requirements• Basic knowledge of the relevant therapeutic area and molecules• Understanding of clinical trials and their design• Strong communication and presentation skills• Ability to work independently and collaboratively• Professionalism and adherence to ethical and regulatory standardsEmployment Options• Full-time position in Pharmaceuticals DivisionWhat We Offer• Opportunity to work in a global pharmaceutical company with a strong focus on innovation• Engagement with leading healthcare professionals and researchers• Professional growth and development within Medical Affairs• Inclusive and diverse work environmentExperience and Skills• Scientific communication and education• Clinical research support and trial understanding• Stakeholder engagement and relationship management• Strategic planning and activity tracking• Collaboration with internal and external teamsCompany OverviewBayer is a global life sciences company with core competencies in health care and agriculture. The Pharmaceuticals division focuses on developing innovative medicines to improve patients’ lives worldwide. Bayer fosters a culture of curiosity, collaboration, and sustainability, aiming to make “Health for all, Hunger for none” a reality.FAQsWhat qualification is required for this role?A degree in natural sciences or a medical qualification (MD/MBBS/BAMS/BDS/MDS).Where is the job located?Kolkata, West Bengal, India.Is clinical experience required?Understanding of clinical trials and basic scientific knowledge in the therapeutic area is required; prior MSL experience is advantageous.What kind of activities will the MSL perform?Scientific engagement with TLs, advisory boards, congresses, and education sessions; reporting and strategy support.Application Tips• Highlight your relevant medical or scientific qualifications• Showcase experience with clinical trials, research dissemination, or medical education• Emphasize strong communication and presentation skills• Demonstrate ability to engage independently with healthcare professionals and teams• Provide examples of previous collaborations or scientific projects, if applicable• Ensure your CV and cover letter clearly address the responsibilities listed in the role

Why This Role MattersRetail pharmacy chains rely on strong operational leadership to maintain consistency, patient safety, and business performance across multiple outlets. A Cluster Manager plays a vital role in ensuring that pharmacy stores operate efficiently while meeting both healthcare and retail standards.This position bridges the gap between corporate management and individual pharmacy outlets by supervising store managers, monitoring inventory levels, ensuring compliance with pharmacy regulations, and driving sales growth.By maintaining operational discipline, supporting staff performance, and improving supply chain efficiency, the Cluster Manager helps retail pharmacy networks deliver reliable healthcare services to communities while ensuring business sustainability.Job DescriptionZeelab Pharmacy Private Limited is hiring a Cluster Manager – Retail Pharmacy in Kolkata to oversee operations across multiple pharmacy outlets. This leadership role focuses on team management, operational performance, and ensuring that each store maintains company standards in customer service, stock management, and compliance.The Cluster Manager will coordinate with store managers, guide pharmacy teams, monitor inventory levels, and ensure efficient supply chain operations across the assigned cluster. The role requires strong leadership abilities, retail pharmacy experience, and operational management skills to support the growth and efficiency of the pharmacy network.Key Features of the Role:• Leadership opportunity managing multiple pharmacy outlets• Direct involvement in retail pharmacy operations and performance management• Responsibility for supervising store managers and pharmacy staff• Exposure to retail sales strategies and supply chain management• Opportunity to drive operational excellence across a pharmacy cluster• Work with a growing pharmacy retail network in KolkataResponsibilities• Oversee daily operations of assigned retail pharmacy outlets to ensure smooth functioning• Ensure all pharmacy stores follow company operational standards and policies• Lead, mentor, and motivate store managers and pharmacy staff• Monitor store performance and work towards achieving sales and revenue targets• Track inventory levels and ensure adequate stock availability across outlets• Coordinate with procurement and supply chain teams for efficient stock management• Implement strategies to improve customer service and patient satisfaction• Monitor compliance with pharmacy regulations and healthcare standards• Analyze store performance metrics and provide regular operational reports• Support training and development initiatives for pharmacy staff• Identify operational challenges and implement solutions for efficiency improvementRequired QualificationsEducational Requirements:• Bachelor’s degree in Pharmacy, Life Sciences, Business Administration, or a related field• Candidates with B.Pharm, M.Pharm, or MBA in Healthcare/Retail Management may be preferredExperience and Skills:• Prior experience in retail pharmacy operations or healthcare retail management• Experience managing multiple stores or supervising pharmacy teams• Strong leadership and team management skills• Knowledge of pharmacy inventory systems and supply chain processes• Understanding of retail pharmacy regulations and compliance requirements• Strong analytical and problem-solving abilities• Excellent communication and organizational skills• Ability to manage multiple locations and operational prioritiesSalary Insights:• Performance incentives, travel allowances, and managerial benefits may also be offeredCompany OverviewZeelab Pharmacy Private Limited is a growing retail pharmacy chain known for providing affordable medicines and healthcare products across India. The company focuses on improving accessibility to quality pharmaceutical products through its expanding network of retail outlets.By combining retail pharmacy operations with healthcare service standards, Zeelab Pharmacy aims to strengthen community healthcare delivery while maintaining efficient supply chains and competitive pricing.FAQsWhat does a Cluster Manager do in retail pharmacy?A Cluster Manager supervises multiple pharmacy outlets, ensuring smooth operations, staff performance, inventory management, and compliance with company standards.Is pharmacy qualification mandatory for this role?While pharmacy qualifications are preferred, candidates with strong retail management experience may also be considered depending on the company’s requirements.How many stores does a Cluster Manager typically manage?The number varies by organization but usually ranges from 5 to 15 pharmacy outlets within a geographic cluster.Is this a field-based role?Yes. Cluster Managers usually travel between pharmacy outlets to monitor operations and support store teams.Application Tips• Highlight experience in managing retail stores or pharmacy operations• Emphasize leadership and team management achievements• Mention experience with inventory management and supply chain coordination• Demonstrate understanding of retail performance metrics and sales targets• Include examples of improving store performance or operational efficiency.

Why This Role MattersClinical trials are essential for developing new medicines, vaccines, and medical treatments. However, the success of these trials depends not only on data collection but also on the accuracy, integrity, and regulatory compliance of the data generated during the research process. This is where Clinical Research Quality Control (QC) Officers play a critical role.Quality Control professionals in clinical research ensure that every stage of a clinical trial follows strict regulatory standards such as International Council for Harmonisation – Good Clinical Practice (ICH-GCP). Their work ensures that clinical trial data is reliable, accurate, and ethically obtained, which ultimately protects patient safety and ensures that research findings are credible.QC Officers act as internal reviewers who verify clinical trial documentation, study records, and regulatory files before they are submitted for audits or regulatory inspections. Their role helps identify errors, inconsistencies, or protocol deviations early in the research process so corrective actions can be implemented promptly.In the clinical research ecosystem, maintaining high-quality data is essential for regulatory approvals and drug development. Without effective quality control processes, clinical trial outcomes may be questioned, which could delay new treatments from reaching patients. Therefore, QC professionals serve as an important safeguard for both research quality and patient safety.For professionals with a background in life sciences, pharmacy, or biotechnology, the role of a Clinical Research QC Officer provides an excellent opportunity to build expertise in regulatory compliance, documentation review, and clinical trial quality assurance.Job DescriptionA leading Clinical Research Organization is hiring a Quality Control (QC) Officer in Kolkata, West Bengal, to support clinical trial quality management and regulatory compliance activities.In this role, the QC Officer will be responsible for reviewing clinical trial documentation, verifying protocol compliance, and ensuring that all clinical research activities align with regulatory standards and Good Clinical Practice guidelines. The position focuses heavily on reviewing study records, verifying data accuracy, and ensuring that clinical documentation meets regulatory expectations. The QC Officer will also support internal quality checks prior to monitoring visits, regulatory audits, and inspections. This includes reviewing essential study documents such as Trial Master Files (TMF), Site Master Files (SMF), and informed consent documentation.Another important responsibility involves collaborating with study teams to identify and resolve discrepancies in clinical trial data. The QC Officer may participate in Root Cause Analysis (RCA) and assist in implementing Corrective and Preventive Actions (CAPA) to address quality issues. Professionals in this role will work closely with clinical research associates, data managers, investigators, and regulatory teams to ensure that clinical trials are conducted according to approved protocols and regulatory guidelines. This role offers valuable experience for professionals who wish to build long-term careers in Clinical Research Quality Assurance, regulatory compliance, and clinical trial management.Key Features of the Role:• Opportunity to work in clinical research quality control and regulatory compliance• Hands-on experience reviewing clinical trial documentation and study records• Exposure to Trial Master File (TMF) and Site Master File (SMF) management• Involvement in CAPA implementation and Root Cause Analysis• Experience preparing clinical trials for regulatory audits and inspections• Career growth opportunities in Clinical Research Quality AssuranceResponsibilities• Perform quality control review of clinical trial documents and source data.• Verify accuracy of data recorded in electronic Case Report Forms (eCRFs).• Ensure compliance with clinical trial protocols and regulatory guidelines.• Review Trial Master File (TMF) and Site Master File (SMF) documentation.• Verify informed consent documentation and regulatory approvals.• Monitor Investigational Product (IP) accountability and storage records.• Conduct internal quality checks prior to monitoring visits or audits.• Identify discrepancies in clinical trial documentation and data records.• Collaborate with study teams to resolve data inconsistencies.• Support Root Cause Analysis (RCA) investigations for quality issues.• Assist in implementing Corrective and Preventive Actions (CAPA).• Maintain documentation required for regulatory inspections and audits.Required Qualifications• Strong knowledge of clinical trial processes and quality control procedures• Understanding of regulatory guidelines including ICH-GCP• Excellent documentation review and analytical abilities• High attention to detail for identifying discrepancies in clinical records• Ability to collaborate effectively with cross-functional clinical research teamsEducational Requirements:• Bachelor’s degree in Life Sciences• Bachelor’s degree in Pharmacy (B.Pharm)• Degree in Biotechnology or related biomedical fieldExperience and Skills:• Experience in clinical trials, site operations, or quality control activities• Familiarity with clinical research documentation and regulatory records• Strong understanding of ICH-GCP guidelines and compliance standards• Experience reviewing clinical trial data and documentation• Ability to perform data verification and documentation quality checks• Knowledge of Root Cause Analysis and CAPA implementation processes• Strong analytical thinking and problem-solving abilities• Effective communication and teamwork skillsSalary InsightsThe estimated salary for Clinical Research QC Officer roles in India typically ranges between ₹3,00,000 and ₹5,50,000 per year, depending on the candidate’s experience, technical skills, and familiarity with clinical research regulations. Additional benefits may include exposure to regulatory audits, professional training in quality assurance processes, and opportunities for advancement within the clinical research industry.Company OverviewClinical Research Organizations (CROs) play an essential role in supporting pharmaceutical companies, biotechnology firms, and medical research institutions in conducting clinical trials. These organizations provide services such as clinical trial monitoring, data management, regulatory support, and quality assurance. By joining a CRO in a quality control role, professionals gain exposure to global clinical research standards and regulatory frameworks. This experience is valuable for building careers in clinical research quality assurance, regulatory affairs, and clinical operations management. Working in the CRO environment also provides opportunities to collaborate with international sponsors, clinical investigators, and healthcare professionals involved in drug development and clinical research.FAQs1. What does a Clinical Research QC Officer do?A QC Officer reviews clinical trial documentation, verifies data accuracy, ensures regulatory compliance, and helps maintain the overall quality of clinical research activities.2. What is the difference between QC and QA in clinical research?Quality Control focuses on reviewing and verifying data and documentation, while Quality Assurance focuses on overall systems, processes, and compliance frameworks.3. Is certification in clinical research required?Certification is not always mandatory but can improve job prospects and demonstrate knowledge of clinical trial processes.4. What career growth opportunities are available after this role?Professionals can progress to Clinical QA Specialist, Senior Quality Auditor, Regulatory Affairs Specialist, or Clinical Project Manager roles.Application Tips• Highlight your knowledge of ICH-GCP guidelines and regulatory compliance.• Include experience related to TMF, SMF, and clinical trial documentation review.• Mention any clinical research certification or training programs.• Showcase your attention to detail and analytical skills.• Emphasize experience with CAPA implementation or Root Cause Analysis.• Ensure your resume reflects experience with clinical trial data verification and quality control processes.

Why This Role MattersClinical research studies generate massive volumes of medical data including patient records, adverse events, medication history, laboratory results, and treatment outcomes. In order for this data to be useful for regulatory submissions, safety monitoring, and scientific analysis, it must be accurately reviewed, standardized, and coded using internationally recognized medical dictionaries.The role of a Clinical Data Coder is essential in transforming raw clinical data into structured and standardized information that can be used for clinical analysis and regulatory reporting. By applying medical coding standards such as MedDRA and WHODD, professionals in this role help ensure that adverse events, medications, and medical histories are categorized consistently across clinical trials.This role supports the entire clinical data lifecycle, from study startup to database lock. Accurate coding allows researchers, statisticians, and regulatory authorities to identify trends, evaluate treatment safety, and make evidence-based decisions during drug development.Professionals working in this role collaborate closely with data management teams, safety teams, clinical research associates, and project managers. Their work directly contributes to maintaining the quality and integrity of clinical trial databases while ensuring compliance with regulatory standards and industry best practices.Job DescriptionThe Clinical Data Coder is responsible for performing clinical data management and medical coding activities that support the successful execution of clinical trials. This role requires reviewing clinical datasets, coding medical terms using standardized dictionaries, validating coding systems, and resolving data queries to maintain data accuracy.The candidate will work within the Data Management team to ensure that coding activities are delivered efficiently while meeting sponsor expectations and regulatory standards. The role may involve serving as a Clinical Data Coder, Lead Coder, or Data Operations Coordinator (DOC) depending on the project requirements.Responsibilities also include supporting coding-related activities across the full clinical study lifecycle, performing quality control procedures, testing coding applications, and assisting with reconciliation of serious adverse events. The role requires strong analytical skills, excellent attention to detail, and a solid understanding of clinical data management processes.The candidate will also collaborate with cross-functional teams, maintain documentation, and ensure that all coding activities comply with company operating procedures and regulatory guidelines.Key Features of the Role:• Exposure to global clinical trial data management processes• Hands-on experience with medical coding dictionaries such as MedDRA and WHODD• Opportunity to work on multiple clinical trial protocols• Involvement in Serious Adverse Event reconciliation activities• Experience with coding validation and quality control procedures• Collaboration with global clinical research teams• Opportunities to take leadership responsibilities in coding projectsResponsibilities• Serve independently as a Clinical Data Coder, Lead Coder, or Data Operations Coordinator for assigned protocols.• Manage delivery of coding activities and standalone coding projects throughout the study lifecycle.• Validate and test coding applications and programming of coding reports.• Test coding-related datasets, edits, and programming activities when required.• Perform data management and coding-related tasks including clinical data review and query resolution.• Write and resolve data clarification queries to ensure data consistency.• Manage coding timelines with guidance from the Data Operations Coordinator or Data Team Lead.• Perform Serious Adverse Event reconciliation activities.• Act as a backup for Lead Coder, Data Operations Coordinator, or Data Team Lead when required.• Conduct quality control checks to ensure high coding accuracy and data integrity.• Assist in implementing new technologies and improvements in coding processes.• Provide coding-related solutions and recommendations to the data management team.• Handle audit requirements for assigned clinical studies and coding projects.• Follow company standard operating procedures and work instructions.• Perform additional tasks assigned by the study team or management.• Maintain strong communication and collaborative working relationships within the team.Required Qualifications• Strong understanding of clinical data management and medical coding processes• Excellent analytical and problem-solving skills• Strong attention to detail when reviewing clinical data• Ability to work independently and manage multiple tasks simultaneously• Strong written and verbal communication skills• Ability to collaborate effectively with cross-functional teamsEducational Requirements:• Bachelor’s degree in Pharmacy, Medicine, Dentistry, Nursing, Life Sciences, or a related healthcare field• Equivalent educational background with relevant training may also be considered• Knowledge of pharmacology, anatomy, and physiology is advantageousExperience and Skills:• Minimum 2 years of experience in clinical data management or medical coding• Strong knowledge of medical terminologies used in clinical research• Experience with medical coding dictionaries such as MedDRA and WHODD• Understanding of the clinical data management lifecycle from study startup to database lock• Familiarity with clinical databases and coding applications• Experience performing data review, query resolution, and reconciliation processes• Knowledge of database technologies related to clinical data management• Strong organizational and leadership abilitiesSalary InsightsClinical Data Coders and Clinical Data Management professionals receive competitive compensation depending on their experience and technical expertise. In addition to salary, employees may receive benefits such as health insurance, performance bonuses, training programs, and opportunities to work on international clinical trials. With experience, professionals can progress to roles such as Senior Clinical Data Coder, Clinical Data Manager, Data Team Lead, or Clinical Project Manager.Company OverviewIQVIA is a global leader in clinical research services, healthcare analytics, and commercial insights for the life sciences and healthcare industries. The company provides advanced data solutions, clinical trial management services, and healthcare intelligence to pharmaceutical, biotechnology, and medical device organizations worldwide.Operating in more than 100 countries, IQVIA combines cutting-edge technology, deep scientific expertise, and extensive healthcare data to accelerate the development and commercialization of innovative medical treatments. The organization supports the full lifecycle of healthcare product development, from clinical trials and regulatory submissions to real-world evidence generation.IQVIA is committed to maintaining the highest standards of integrity, quality, and innovation while helping improve patient outcomes and population health globally.FAQs1. What does a Clinical Data Coder do?A Clinical Data Coder reviews clinical trial data and converts medical terms into standardized codes using dictionaries like MedDRA and WHODD.2. What skills are important for this role?Knowledge of medical terminology, attention to detail, analytical skills, and understanding of clinical data management processes are essential.3. Is clinical research experience required?Yes, most roles require at least two years of experience in clinical data management or medical coding.4. What are the career growth opportunities?Professionals can advance to Senior Data Coder, Clinical Data Manager, Data Team Lead, or Clinical Project Manager roles.Application Tips• Highlight your knowledge of medical terminology, pharmacology, anatomy, and physiology in your resume.• Clearly mention experience with medical coding dictionaries such as MedDRA and WHODD.• Include your experience in clinical data review, query resolution, and data reconciliation.• Emphasize familiarity with clinical databases and data management systems.• Demonstrate your attention to detail and ability to manage clinical datasets accurately.• Mention any experience working in clinical research teams or global study environments.• Keep your resume structured and highlight clinical data management skills relevant to the role.

Why This Role MattersThe Pharmacist – Warehouse Operations plays a critical role in ensuring safe, compliant, and efficient pharmaceutical distribution processes. This position ensures proper stock management, regulatory compliance, and adherence to quality standards within the warehouse environment.By maintaining accurate documentation, ensuring FIFO/FEFO compliance, and coordinating with internal teams, the role directly supports uninterrupted supply chain operations and patient safety.Job DescriptionA reputed pharmaceutical distribution organization is hiring a licensed Pharmacist for its warehouse operations in Kolkata. The selected candidate will be responsible for managing pharmaceutical inventory, maintaining regulatory compliance, supporting billing and documentation processes, and ensuring smooth coordination across supply chain functions. This is a full-time position requiring a valid and active pharmacist license.Key Features of the Role• Position: Pharmacist – Warehouse• Location: Kolkata• Experience Required: 6 months – 1 year• Industry: Pharmaceutical Distribution / Supply Chain• Employment Type: Full-Time• License: Valid and active Pharmacist License (Mandatory)• Salary: ₹25,000 – ₹35,000 per monthKey ResponsibilitiesWarehouse & Inventory Management• Manage stock inward/outward operations• Handle STN, GRN, sales orders, credit notes, and billing• Ensure proper storage and batch control• Maintain FIFO/FEFO compliance• Monitor expiry management and stock reconciliationDocumentation & Reporting• Maintain accurate inventory records• Prepare daily MIS reports• Ensure compliance with QMS and SOP requirements• Maintain regulatory documentation as per guidelinesCoordination & Quality Compliance• Handle customer and dealer queries• Coordinate for timely dispatch of goods• Report non-conformities and product complaints to QA within 24 hours• Ensure adherence to regulatory requirementsSafety & Housekeeping• Follow EHS guidelines• Maintain warehouse safety standards• Ensure proper housekeeping practicesRequired QualificationsEducational Background:• Bachelor of Pharmacy (B.Pharm) or Diploma in Pharmacy (with valid registration)Experience:• 6 months to 1 year experience in pharmaceutical warehouse distribution or supply chain operationsTechnical Skills (Preferred):• Knowledge of pharmaceutical storage and regulatory compliance• Understanding of QMS, SOPs, FIFO/FEFO systems• Experience with ERP and inventory management software• Strong proficiency in MS Excel (Mandatory)Core Skills:• Attention to detail• Organizational skills• Basic accounting and billing knowledge• Good communication and coordination skillsSalary InsightsThe salary range for this role is ₹25,000 – ₹35,000 per month, depending on experience and skill level.FAQsQ1. Is pharmacist license mandatory?Yes, a valid and active pharmacist license is required.Q2. Is prior warehouse experience necessary?Yes, 6 months to 1 year of experience in pharmaceutical warehouse or supply chain operations is required.Q3. Is MS Excel knowledge mandatory?Yes, proficiency in MS Excel is mandatory for reporting and data management.Q4. Is this a field job?No, this is a warehouse-based operational role.Q5. Is this a full-time position?Yes, this is a full-time employment opportunity.Application Tip• Mention your pharmacist registration number clearly• Highlight warehouse or distribution experience• Specify ERP software exposure• Showcase FIFO/FEFO and QMS knowledge• Emphasize Excel reporting skills

Why This Role MattersThe role of a Staff Nurse in homecare is a beacon of hope for individuals and families in need of compassionate and skilled care. As a critical member of our homecare team, you will have the opportunity to make a profound impact on the lives of our patients. Your dedication, expertise, and empathy will empower patients to regain control over their health, allowing them to live more independently and with dignity. By joining our team, you will become part of a mission-driven organization that prioritizes the well-being of our patients and their families, recognizing the value of each individual's life and dignity.Job DescriptionWe are seeking dedicated and compassionate Staff Nurses to join our homecare team in Delhi / NCR, Kolkata, and Bengaluru. As a Staff Nurse, you will be responsible for providing high-quality, patient-centered care in the comfort of patients' homes. Your expertise will encompass various aspects of nursing practice, including assessments, medication administration, wound care, and education of patients and their families. You will work collaboratively with multidisciplinary teams to ensure seamless care transitions and optimize patient outcomes.Provide comprehensive nursing care to patients in their homes, adhering to individualized care plans.Conduct thorough assessments, identifying patients' needs and developing strategies to address them.Administer medications, treatments, and therapies as prescribed by physicians.Monitor patients' conditions, reporting changes to healthcare providers and making recommendations for adjustments in care plans.Collaborate with patients, families, and healthcare teams to ensure continuity of care and coordination of services.Key ResponsibilitiesAs a Staff Nurse, you will be responsible for the following key areas:Nursing Care PlanningYou will be responsible for developing, implementing, and evaluating individualized care plans that address patients' physical, emotional, and social needs. This will involve conducting thorough assessments, identifying patients' strengths and weaknesses, and developing strategies to promote optimal health outcomes.Medication ManagementYou will be accountable for administering medications, treatments, and therapies as prescribed by physicians. This will involve carefully monitoring patients' responses to medications, reporting any adverse reactions, and making recommendations for adjustments in medication regimens.Wound CareYou will be responsible for providing wound care services, including dressing changes, wound cleaning, and applying topical treatments. This will involve working closely with patients and their families to educate them on wound care techniques and promoting self-care practices.Patient EducationYou will be accountable for educating patients and their families on various aspects of health and wellness, including disease management, nutrition, and self-care practices. This will involve developing and implementing patient education plans that are tailored to individual patients' needs and abilities.Required QualificationsTo be considered for this role, you must possess the following qualifications:Basic Life Support (BLS) Certification Registered Nurse (RN) LicenseMinimum 0-5 years of experience in homecare or hospital settingsExcellent communication and interpersonal skillsAbility to work independently and as part of a teamFamiliarity with electronic health records (EHRs) and other healthcare technologiesSalary InsightsThe salary for this role is competitive and commensurate with experience. In Delhi / NCR, the salary range for Staff Nurses is approximately ₹15,000 - ₹25,000 per month. In Kolkata, the salary range is approximately ₹12,000 - ₹20,000 per month. In Bengaluru, the salary range is approximately ₹18,000 - ₹30,000 per month. Factors affecting salary include experience, qualifications, and location.Career Growth PathAs a Staff Nurse, you will have opportunities for career growth and advancement within our organization. With experience, you can progress to senior roles such as Charge Nurse, Clinical Nurse Specialist, or Nurse Manager. To support your growth, we offer various training programs, mentorship opportunities, and education assistance.About Apollo Health ResourcesApollo Health Resources is a leading healthcare organization that provides high-quality homecare services to patients in Delhi / NCR, Kolkata, and Bengaluru. Our mission is to deliver compassionate, patient-centered care that empowers individuals to regain control over their health and live more independently. We prioritize the well-being of our patients and their families, recognizing the value of each individual's life and dignity. Our work culture is collaborative, supportive, and mission-driven.Frequently Asked QuestionsQ: What is the eligibility criteria for this role?A: To be eligible for this role, you must possess a Registered Nurse (RN) license, Basic Life Support (BLS) certification, and a minimum 0-5 years of experience in homecare or hospital settings.Q: What is the salary range for this role?A: The salary range for this role varies by location, with approximate ranges of ₹15,000 - ₹25,000 per month in Delhi / NCR, ₹12,000 - ₹20,000 per month in Kolkata, and ₹18,000 - ₹30,000 per month in Bengaluru.Q: How can I apply for this role?A: To apply for this role, please submit your resume and cover letter to [insert contact information].Q: What is the work culture like at Apollo Health Resources?A: Our work culture is collaborative, supportive, and mission-driven. We prioritize the well-being of our patients and their families, recognizing the value of each individual's life and dignity.Q: Are there opportunities for career growth and advancement within the organization?A: Yes, there are opportunities for career growth and advancement within our organization. With experience, you can progress to senior roles such as Charge Nurse, Clinical Nurse Specialist, or Nurse Manager.Application TipsTo increase your chances of being selected for this role, we recommend the following application tips:Tailor your resume and cover letter to the job descriptionHighlight your relevant healthcare skills and experienceUse keywords from the job description in your application Showcase your passion for patient-centered care and commitment to our mission

Why This Role MattersThe Physiotherapist plays an important role in delivering quality rehabilitation services to patients requiring neurological and orthopaedic care. This position provides early-career professionals with structured clinical exposure while contributing to improved patient mobility, recovery, and functional independence.Job DescriptionRoy Physiocare is hiring a Full-Time BPT Physiotherapist (Freshers Welcome) for its locations in Ariadaha and Baranagar, Kolkata, West Bengal. The role involves assisting in neurological and orthopaedic rehabilitation programs, gaining hands-on clinical experience, and participating in structured training under professional supervision. Immediate joining is preferred.Key Features of the Role• Position: Physiotherapist (BPT – Fresher Welcome)• Company: Roy Physiocare• Location: Ariadaha & Baranagar, Kolkata, West Bengal• Employment Type: Full-Time, Permanent• Experience Level: Fresher / Entry-Level• Salary: ₹15,000 – ₹18,000 per Month• Specialization Exposure: Neurological & Orthopaedic RehabilitationResponsibilities• Assess patients under supervision and assist in treatment planning• Deliver physiotherapy sessions for neurological and orthopaedic cases• Support rehabilitation programs using advanced rehab technologies• Monitor patient progress and maintain basic documentation• Participate in structured clinical training programs• Ensure patient comfort and safety during therapy sessionsRequired Qualification• Bachelor of Physiotherapy (BPT)Educational Requirement• BPT from a recognized institutionImportant Remarks• Freshers are encouraged to apply• Immediate joining preferred• Strong clinical interest and positive attitude required• Willingness to learn and adapt to structured training environment• Performance-based growth opportunities availableWhat We Offer• Structured clinical training• Exposure to neurological and orthopaedic rehabilitation• Hands-on experience with advanced rehabilitation technologies• Performance-based growth pathway• Opportunity for long-term career developmentExperience and Skills• Basic knowledge of physiotherapy assessment and treatment• Interest in neuro and orthopaedic rehabilitation• Strong learning mindset• Good communication and patient-handling skills• Ability to work as part of a clinical teamSalary Insights• ₹15,000 – ₹18,000 per month• Salary based on performance and clinical attitudeCompany OverviewRoy Physiocare is a physiotherapy clinic based in Kolkata, West Bengal, offering rehabilitation services with a focus on neurological and orthopaedic care. The clinic emphasizes structured training, hands-on experience with advanced technologies, and performance-based professional growth for its team members.FAQsWho can apply?Candidates with a BPT degree, including freshers.Is this a part-time role?No, this is a full-time permanent position.What is the salary range?₹15,000 – ₹18,000 per month.Is experience mandatory?No, freshers are welcome to apply.How do I apply?Apply through the Indeed job link below.Application Tips• Highlight internship or clinical training exposure• Mention interest in neuro and orthopaedic rehabilitation• Emphasize willingness to learn and grow• Keep your resume clear and structured• Be ready for immediate joining if shortlisted

Why This Role MattersThe clinical research industry in India is expanding rapidly, increasing demand for skilled professionals in business development within CROs and biotechnology organizations. This role plays a critical part in building strategic partnerships, driving revenue growth, and expanding access to clinical trials and biospecimen research services.Indoriv Clinical Private Limited operates at the intersection of biotechnology and clinical research. As a Business Development Executive, you will contribute directly to strengthening collaborations with hospitals, pharmaceutical companies, and research institutions.This opportunity is ideal for professionals looking to build a long-term career in clinical research business development, especially within the biospecimen and CRO sector.Job DescriptionIndoriv Clinical Private Limited is hiring a Business Development Executive in Kolkata for a field-focused role centered on partnerships in clinical trials and human biospecimen research.The selected candidate will be responsible for generating new business opportunities, maintaining client relationships, and supporting revenue growth initiatives within the clinical research ecosystem.This role requires strong communication skills, industry knowledge, and a target-driven mindset.Key Features of the Role• Field-intensive business development role• Exposure to clinical trials and biospecimen research• Opportunity to collaborate with hospitals and pharma companies• Performance-based incentives structure• Growth-oriented role in biotechnology CRO sector• Direct interaction with healthcare professionals and researchersResponsibilities Required• Developing partnerships with hospitals, CROs, pharma companies, and research institutions• Generating new leads for clinical trials and biospecimen procurement• Driving revenue growth through strategic business development initiatives• Understanding client requirements and aligning company services accordingly• Collaborating with clinical, laboratory, and operations teams• Representing the organization at industry conferences and networking meetings• Maintaining CRM records and tracking sales performance• Achieving assigned revenue and business growth targetsQualificationsCandidates must possess one of the following qualifications:• Bachelor’s degree in Life Sciences• Bachelor’s degree in Biotechnology• Bachelor’s degree in Pharmacy• Bachelor’s or Master’s degree in Business Administration• Degree in related healthcare or scientific disciplineEducational Requirements• Full-time degree from a recognized university• Academic background in life sciences, biotechnology, or healthcare preferred• Business or marketing specialization will be an added advantageExperience and SkillsExperience• 1–2 years of experience in business development or healthcare sales• Experience in clinical research sales preferred• Exposure to biotech partnerships will be advantageousSkills Required• Strong communication and negotiation skills• Relationship-building ability with doctors and researchers• Understanding of clinical research and biospecimen processes• Target-driven and revenue-focused mindset• CRM handling and lead management skills• Willingness to travel for field visits• Professional networking capabilitiesSalary InsightsEstimated Salary Range• ₹3.5 – ₹5.5 LPA (based on experience and performance)Additional Benefits:• Performance-linked incentives• Exposure to global clinical research projects• Career growth opportunities within CRO industry• Collaborative biotechnology work culture• Industry networking exposureCompany OverviewIndoriv Clinical Private Limited is a hybrid biotechnology Contract Research Organization (CRO) specializing in:• Human specimen biobanking• Prospective clinical trials• Global biospecimen supply• High-integrity biological sample managementThe organization supports pharmaceutical companies, hospitals, and research institutions by providing high-quality biological samples compliant with regulatory and ethical standards.Working at Indoriv Clinical offers structured exposure to biotech operations, clinical trial partnerships, and international research collaborations.FAQsIs this a field-based role?Yes, this is a field-intensive business development position.Is prior clinical research experience mandatory?Preferred but not mandatory. Healthcare sales experience is also considered.Is travel required?Yes, candidates must be willing to travel within the assigned territory.What growth opportunities are available?Career progression into Senior Business Development Executive or Business Development Manager roles.Location of posting?Kolkata, West Bengal.Application Tips• Research basics of clinical trials and biospecimen management• Understand CRO business models• Prepare examples of sales targets achieved• Highlight healthcare networking experience• Demonstrate strong negotiation and communication skills• Be ready to discuss territory development strategies

Why This Role MattersThe Prosthetist and Orthotist at Evolution Healthcare Pvt. Ltd. plays a crucial role in improving patient mobility, function, and quality of life through the design, fitting, and management of prosthetic and orthotic devices. This position focuses on delivering personalised care, conducting assessments, and providing rehabilitation solutions for patients with limb loss, musculoskeletal impairments, or mobility challenges.Job DescriptionThe Prosthetist and Orthotist will assess patients’ physical conditions, design and fit prosthetic and orthotic devices, and provide ongoing follow-up care to ensure comfort, function, and safety. Responsibilities include collaborating with physiotherapists and rehabilitation teams, educating patients on device use and maintenance, and maintaining accurate clinical documentation. The role requires a combination of technical expertise, clinical reasoning, and patient-centred care.Key Features of the Role• Position: Prosthetist and Orthotist• Company: Evolution Healthcare Pvt. Ltd.• Location: Kolkata, West Bengal, India• Employment Type: Full-Time• Salary: Not Disclosed• Work Environment: Rehabilitation and Prosthetics/Orthotics ClinicResponsibilities• Conduct thorough assessments of patients requiring prosthetic and orthotic devices• Design, fabricate, and fit customised prostheses and orthoses• Provide education and training to patients on device usage, maintenance, and safety• Monitor patient progress and make adjustments to devices as needed• Collaborate with physiotherapists, occupational therapists, and rehabilitation teams• Maintain accurate clinical records and documentation• Ensure compliance with professional and ethical standards in device provision• Participate in continuous professional development to stay updated on advancements in prosthetics and orthoticsRequired QualificationCandidates must hold a recognised degree in Prosthetics and Orthotics and demonstrate competency in patient assessment and device fitting. Certification is preferred but not mandatory.Educational Requirement• Bachelor’s Degree in Prosthetics & Orthotics• Relevant certification preferred• Knowledge of clinical rehabilitation principles and assistive device technologyImportant Remarks• Strong patient-centred approach essential• Technical skills in fabrication, fitting, and adjustment of devices required• Excellent communication and interpersonal skills required• Ability to work collaboratively within a rehabilitation teamExperience and SkillsExperience Required• Clinical experience in prosthetics and orthotics preferred• Fresh graduates with strong training and internship exposure may be consideredKey Skills Expected• Competence in assessment, design, and fitting of prosthetic and orthotic devices• Strong problem-solving and clinical reasoning abilities• Ability to educate and counsel patients effectively• Attention to detail and precision in device fabrication and adjustments• Professionalism and teamwork in multidisciplinary settingsSalary Insights• Salary not disclosed• Compensation aligned with rehabilitation and prosthetics/orthotics industry standards in IndiaCompany OverviewEvolution Healthcare Pvt. Ltd. is a Kolkata-based healthcare provider specialising in prosthetics, orthotics, and rehabilitation services. The company emphasises personalised patient care, technical excellence, and continuous professional development for healthcare professionals in assistive device management.FAQs1. What qualification is required for this role?Bachelor’s degree in Prosthetics & Orthotics; certification preferred.2. Can fresh graduates apply?Yes, fresh graduates with relevant training or internship experience may be considered.3. What type of patients will I work with?Patients requiring prosthetic limbs, orthotic supports, or rehabilitation for mobility impairments.4. Where is the clinic located?Kolkata, West Bengal, India.5. Is certification mandatory?Certification is preferred but not mandatory.Application Tips• Highlight any clinical internships or projects in prosthetics and orthotics• Emphasise technical skills in device design, fitting, and adjustment• Showcase patient-centred care and communication skills• Include measurable outcomes from previous rehabilitation cases• Tailor your CV to reflect competency in prosthetic and orthotic services

Roles & Responsibilities• Dispense medications accurately as per prescription and regulatory standards• Verify prescriptions for dosage, drug interactions, and patient safety• Counsel patients on medication usage, side effects, and storage• Ensure compliance with pharmacy laws and internal SOPs• Maintain inventory, stock levels, and expiry monitoring• Handle billing, documentation, and daily operational records• Supervise pharmacy operations and support junior staff (for Sr. Pharmacist / ATL roles)• Drive team performance, ensure service quality, and manage shift operations (for ATL)Qualification• B.Pharm (Bachelor of Pharmacy) / D.Pharm (Diploma in Pharmacy)• Valid State Pharmacy License (Registered Pharmacist)Experience• Freshers can apply• 1–2 years for Pharmacist (Experienced)• 2–4 years for Senior Pharmacist• 4–6 years for ATL / Team LeadSalary (CTC per month)• Freshers: ₹18,000• 1–2 Years: ₹22,000 – ₹24,000• 2–4 Years (Senior Pharmacist): ₹25,000 – ₹26,000• 4–6 Years (ATL): ₹30,000 – ₹33,000• 6+ Years: ₹33,000+Skills• Accuracy in dispensing and prescription verification• Strong patient counseling and communication skills• Knowledge of pharmacy regulations and compliance• Inventory and operational management skills• Leadership and team coordination abilities (for Senior/ATL roles)About the CompanyTata 1mg is a leading digital healthcare platform in India, offering online pharmacy, diagnostics, and teleconsultation services. The company focuses on making healthcare accessible, affordable, and reliable through technology-driven pharmacy and retail operations.

Roles and Responsibilities:• Provide remedial massage therapy treatments in a busy clinic setting.• Deliver high-quality services aligned with clinic standards and signature treatments.• Collaborate with massage therapists, bodyworkers, and acupuncturists.• Maintain professional, ethical, and eco-conscious practice standards.• Participate in ongoing training and skill development.• Foster a positive, harmonious, and client-centered environment.Work Schedule:• Flexible working arrangements.• Weekday and weekend shifts available.• Minimum commitment of at least 2 half-days per week (more preferred).Qualification:• Relevant qualification in Remedial Massage Therapy.• Professional certification/licensure as required.Experience:• Prior clinical or wellness experience preferred.• Experience in a team-based therapy setting is an advantage.Skills:• Strong remedial massage techniques.• Excellent interpersonal and communication skills.• Professionalism, kindness, and teamwork orientation.• Passion for continued learning and holistic wellness.About the Clinic:Willow Massage & Wellness is a wellness clinic in Howrah offering massage therapy, bodywork, and acupuncture services. The clinic values kindness, community, eco-conscious practices, professionalism, and continuous learning in a supportive environment.

Roles and Responsibilities:• Conduct patient assessments, diagnosis, and treatment planning for physical rehabilitation.• Develop and implement personalized physiotherapy treatment programs.• Provide exercise therapy and rehabilitation strategies to improve patients' physical capabilities.• Monitor and evaluate patient progress, modifying treatment plans as required.• Collaborate with other healthcare professionals to ensure comprehensive patient care.• Maintain accurate and up-to-date patient records and clinical documentation.• Follow established clinical care protocols and ensure a patient-focused environment.Qualification:• Bachelor’s or Master’s Degree in Physiotherapy or relevant certification in Physiotherapy.Experience:• Previous experience in a clinical setting is preferred.Skills:• Practical expertise in physiotherapy treatments and patient assessments.• Strong knowledge of exercise therapy planning and rehabilitation techniques.• Understanding of anatomy, physiology, and clinical care protocols.• Excellent communication and interpersonal skills.• Ability to work effectively in an on-site clinical environment.About the Company:Getphysio is a physiotherapy service provider operating in Kolkata, associated with specialty physiotherapy and hydrotherapy clinics. The organization focuses on delivering patient-centered rehabilitation services through structured assessment, personalized treatment planning, and professional clinical care.

Roles and Responsibilities:• Assess patients and evaluate their physical conditions thoroughly.• Develop and implement personalized physiotherapy treatment plans.• Conduct physical therapy sessions using appropriate therapeutic exercises and techniques.• Monitor patient progress and modify treatment plans as required.• Collaborate with other healthcare professionals to ensure comprehensive patient care.• Educate patients on post-treatment care, rehabilitation exercises, and preventive measures.• Maintain accurate patient records and clinical documentation.• Ensure high standards of patient care, safety, and confidentiality.Qualification:• Bachelor’s or Master’s Degree in Physiotherapy from a recognized institution.• Valid licensure or certification as required by regional healthcare authorities.Experience:• Previous experience in clinical or physical therapy roles is highly desirable.Skills:• Strong knowledge of musculoskeletal conditions, rehabilitation methods, and pain management.• Proficiency in patient assessment and treatment planning.• Excellent communication and interpersonal skills.• Ability to work collaboratively in a multidisciplinary healthcare team.• Compassionate, patient-focused approach with commitment to quality care.About the Company:Alexa Healthcare India Pvt Ltd, operating as Alexa Physiotherapy Clinic, is a Newtown-based healthcare provider in Kolkata specializing in personalized, non-surgical, drug-free physiotherapy care. Equipped with modern modalities, the clinic offers both in-clinic and at-home treatment services. Led by Dr. Shipra Kumari, the organization is dedicated to restoring mobility, relieving pain, and enhancing overall wellness through hands-on therapy and individualized treatment plans.

Roles & Responsibilities• Conduct Site Selection Visits (SSV), Site Initiation Visits (SIV), Interim Monitoring Visits (IMV), and Close-Out Visits (COV)• Ensure clinical trials are conducted in compliance with ICH-GCP guidelines, SOPs, and applicable regulatory requirements• Monitor study progress to ensure adherence to approved protocol, timelines, and quality standards• Perform Source Data Verification (SDV) and validate CRF/eCRF entries for accuracy and completeness• Identify, document, and follow up on protocol deviations, discrepancies, and corrective actions• Maintain, review, and update Trial Master File (TMF) documentation• Ensure proper informed consent process compliance and documentation• Coordinate with investigators, site staff, CROs, and sponsors for smooth study execution• Track, review, and report Serious Adverse Events (SAEs) as per regulatory timelines• Prepare detailed monitoring visit reports and follow-up letters• Support audit and inspection readiness by ensuring documentation accuracy and completeness• Assist in regulatory submissions and essential document managementQualification• B.Pharm (Bachelor of Pharmacy) / M.Pharm (Master of Pharmacy)• BSc / MSc in Life Sciences, Clinical Research, or related disciplineExperience• 1–2 years of hands-on experience in clinical trial monitoring• Working knowledge of ICH-GCP guidelines• Experience in TMF maintenance and SAE reportingSkills• Strong clinical trial monitoring expertise• Proficiency in Source Data Verification (SDV)• Experience with eCRF documentation and review• Strong understanding of regulatory compliance frameworks• Excellent documentation and reporting skills• Strong communication and site coordination abilities• Ability to manage multiple study activities efficiently• High attention to detail and quality-focused approachAbout the OrganizationDesun Hospital is a multi-specialty healthcare institution in Kolkata with a structured clinical research environment. The hospital provides opportunities for clinical research professionals to gain hands-on experience in monitoring, regulatory compliance, and investigator coordination within a hospital-based research setup.

Roles & Responsibilities• Communicate fair and balanced therapeutic area-related, product-related, and clinical information to external stakeholders.• Execute the scientific engagement plan in alignment with the Therapy Medical Plan.• Develop long-term relationships with opinion leaders and relevant stakeholders.• Respond to unsolicited requests for medical information, including off-label data related to marketed and pipeline products.• Provide clinical and medical presentations to external stakeholders.• Support ongoing and future Medical Affairs Company-Sponsored Studies, including site reviews and feedback.• Assist in the development and support of national disease registries and Real-World Evidence (RWE) projects.• Maintain up-to-date knowledge of scientific/medical developments and share insights to develop field medical plans.• Provide medical expertise to internal teams like sales and market access.• Support market access strategies at the regional level, including hospital listings.• Ensure compliance with internal and external regulations, prioritizing patient safety.Qualification• MBBS/MD or equivalent medical degree.• Minimum 1-2 years of working experience in oncology.Experience• 1 - 3 years of experience in Medical Science Liaison or Medical Affairs, specifically in oncology.Vacancies• 3 Medical Science Liaison positions available in Delhi, Kolkata, and Chennai.Skills• Strong communication and presentation skills.• Ability to build and maintain relationships with opinion leaders and healthcare professionals.• Proficiency in English.• Strong business acumen and autonomy in managing priorities.• Leadership, emotional intelligence, active listening, and negotiation skills.• Ability to manage cross-functional projects effectively.• Knowledge of compliance regulations and scientific integrity.About the CompanyThis role is for a Global Pharmaceutical MNC that is dedicated to advancing science and ensuring access to healthcare worldwide. The company specializes in providing innovative medicines to treat hard-to-treat cancers and is committed to enhancing patient outcomes through scientific exchange, clinical research, and market access strategies.

Roles & responsibilities:• Provide post-marathon stretching and physiotherapy support for athletes• Assist in yoga and rehabilitation exercises• Support participants in improving mobility, flexibility, and recovery• Maintain safety and hygiene standards during sessions• Gain hands-on practical experience in sports and physiotherapyQualification:• Fresher physiotherapy or yoga students welcome• Relevant educational background in physiotherapy, yoga, or sports therapy preferredExperience:• Practical exposure providedSkills:• Basic physiotherapy and yoga knowledge• Ability to guide stretching and exercises safely• Good communication and interpersonal skills• Willingness to work with athletes and in a team environmentBenefits:• Food providedAbout the company:Keralian Wellness is a wellness and rehabilitation organization in Kolkata that focuses on fitness, physiotherapy, and yoga services. The company provides practical experience opportunities for freshers and emphasizes holistic health, recovery, and sports rehabilitation.

Roles & Responsibilities• Perform medical surveillance and pharmacovigilance case processing activities• Review, assess, and medically code adverse event reports• Conduct medical review of ICSRs (Individual Case Safety Reports)• Ensure compliance with regulatory requirements and internal SOPs• Support signal detection activities and safety data analysis• Maintain accurate documentation, reporting, and audit readinessQualification• Pharm D (Doctor of Pharmacy)• BDS / MDS• BHMS• BAMSExperience• Fresh graduates eligibleSkills• Good understanding of medical terminology• Strong analytical and assessment skills• Effective communication and documentation abilities• Interest in pharmacovigilance, drug safety, and medical surveillanceAbout the OrganizationIQVIA – A global human data science company providing advanced analytics, technology solutions, and clinical research services, offering hybrid work opportunities and global exposure in pharmacovigilance and drug safety.Interested and eligible candidates can send their updated resume to: Email: pavan.cm@iqvia.com

Roles & responsibilities:• Assess clients’ health and wellness needs and create personalized wellness plans• Guide clients on implementing strategies that promote long-term health and vitality• Educate clients on recovery techniques, performance enhancement, and lifestyle changes• Monitor client progress to ensure optimal outcomes• Deliver exceptional customer service and maintain client relationshipsQualifications:• MBBS or Bachelor’s degree or equivalent experience in a health-related discipline• Background in nutrition, physiotherapy, exercise science, or related field is a plusExperience:• Not specifiedSkills required:• Strong knowledge and experience in health and wellness, longevity strategies, and recovery therapies• Excellent communication, client engagement, and interpersonal skills• Ability to assess individual needs and design personalized wellness and performance plans• Enthusiasm for promoting long-term health and optimizing performanceAbout the company:Evity Wellness is a social wellness club offering next-generation recovery and performance therapies to help individuals build strength, stay healthy, recover fully, and achieve peak performance. The company focuses on long-term vitality and wellness for improved daily living.

Roles & Responsibilities:• Review, assess, and process safety data in compliance with regulatory requirements.• Perform pharmacovigilance activities including AE intake, triage, and case processing.• Enter and manage safety cases in safety databases with accurate documentation.• Perform MedDRA coding, product coding, and narrative writing.• Handle literature case processing and follow-up activities.• Ensure adherence to SOPs, internal guidelines, and quality standards.• Meet defined productivity, quality, and turnaround time metrics.• Attend project meetings and escalate issues to senior team members when required.• Complete mandatory trainings within defined timelines.Qualification:• Bachelor’s degree in Pharmacy, Life Sciences, or a related healthcare discipline• B. Pharm / M. Pharm (Preferred)Experience:• Freshers interested in Drug Safety / Pharmacovigilance• Prior exposure or interest in Pharmacovigilance / Drug Safety will be an advantageSkills:• Good knowledge of medical terminology• Strong written and verbal communication skills• Working knowledge of MS Office and web-based applications• High attention to detail and time management skills• Ability to work independently and within a team• Willingness to work in shiftsAbout the Organization:IQVIA is a global leader in clinical research, pharmacovigilance, and healthcare intelligence, providing advanced analytics, technology solutions, and clinical services to the life sciences industry, and offering strong career growth opportunities for professionals entering the drug safety and regulatory domain.

ROLE & RESPONSIBILITIES:• Assess children’s developmental needs using standardized occupational therapy tools• Plan and implement individualized therapeutic intervention programs• Address developmental delays and disabilities through structured therapy sessions• Monitor, evaluate, and document patient progress regularly• Collaborate with parents, caregivers, educators, and multidisciplinary teams• Provide guidance and support to families for consistent home-based interventions• Maintain detailed and accurate therapy records and reports• Support professionals through guidance and collaborative care planningQUALIFICATION:• Degree or certification in Occupational Therapy or a related field• Valid registration/licensure as per professional requirementsEXPERIENCE:• Experience working with children with developmental delays or disabilities is preferredSKILLS:• Strong expertise in Occupational Therapy and Rehabilitation• Knowledge of Pediatrics and child development• Excellent communication and interpersonal skills• Empathy, patience, and ability to build rapport with children and families• Ability to work effectively within multidisciplinary teamsABOUT THE COMPANY:Mom’s Belief is a child-focused organization committed to holistic development through early awareness and targeted intervention. Using a multidisciplinary approach, standardized clinical methods, and flexible online and offline programs, Mom’s Belief empowers children with developmental delays and disabilities to achieve their full potential while supporting parents, educators, and caregivers at every step.