Mumbai Healthcare Jobs

Roles & Responsibilities• Perform batch documentation review and support batch release activities for products listed on Aspire Pharma’s MIA and third-party MIAs• Review stability data and ensure compliance with approved specifications• Manage deviations, non-conformances, CAPAs, and change control activities• Support MIA product setup, batch release documentation, and launch readiness activities• Conduct monthly compliance checks and contribute to product launch activities• Maintain up-to-date knowledge of EU/UK GxP regulations, including GMP, GDP, GVP, and GCP• Ensure compliance with regulations related to medical devices (ISO 9001, ISO 13485, ISO 14971), controlled drugs, nutritional products, GDPR, and the UK Data Protection Act• Communicate effectively with internal teams, vendors, and customers to implement regulatory changes• Investigate non-conformances and deviations and support corrective and preventive actions• Monitor vendor performance to ensure compliance and supply continuity• Update quality procedures and documentation in line with legislative and regulatory requirementsQualification• Bachelor’s degree in Science or related disciplineExperience• 5–8 years of relevant experience in Quality Assurance or Technical Compliance (desirable)• Experience with MIA batch review and release activities (desirable)• Strong understanding of pharmaceutical regulatory and compliance requirementsSkills• Excellent written and spoken English communication skills• Strong time management and organizational abilities• High attention to detail and documentation accuracy• Proactive team player with problem-solving mindset• Proficiency in MS Office (Word, Excel, Outlook)• Experience with Adobe Acrobat and electronic signature tools (desirable)• Familiarity with Q-Pulse or other electronic QMS systems (desirable)About the CompanyAspire Pharma is a UK-based asset-light pharmaceutical manufacturer with a diversified portfolio of over 250 products across urology, ophthalmology, CNS, dermatology, and specialty generics, delivering innovative and reliable healthcare solutions to underserved markets worldwide.

Roles & Responsibilities• Assist in preparation and review of aggregate safety reports, risk management plans, and signal detection activities• Generate outputs and reports from safety databases and systems• Support data requests, sales data calculations, regulatory website searches, and report planning activities• Author full or partial sections of global regulatory safety documents, including: Annual Reports (IND and others), PSUR / PADER / PBRER, DSUR, Risk Management Plans (RMPs)• Develop assigned report sections using templates, reused content, and low to medium complexity safety analyses• Review and annotate line listings, prepare case narratives, and summarize safety data per approved strategies• Participate in comment resolution and report finalization discussions• Support signal detection activities, including data cleaning, line listing review, and preparation of signal review materials• Assist in preparing ad hoc safety reports, safety issue analyses, and label update justifications• Write sections of Common Technical Document (CTD) summaries, including Clinical and Non-Clinical Overviews• Conduct literature searches and screen publications for relevance to safety reports• Prepare literature abstracts and summaries for regulatory documentation• Ensure compliance with SOPs, regulatory requirements, GVP, and ICH-GCP guidelines• Promote consistent, efficient, and high-quality writing processes to meet project timelines• Maintain high standards of customer service and effective collaboration with internal and external stakeholdersQualification• Bachelor’s degree in Life Sciences or equivalent• Advanced degree (Master’s or PhD) preferredExperience• Excellent written and spoken English skills• Strong organizational and time management abilities• Scientific or clinical research experience is desirable• Knowledge of pharmacovigilance, regulatory requirements, and ICH-GCP guidelines preferred• Around 2 years of experience in medical writing or the pharmaceutical industry is an advantageSkills• Proficiency in MS Word, PowerPoint, and Excel• Strong analytical and documentation skills• Ability to manage multiple deliverables under timelines• Excellent interpersonal and communication skillsAbout the CompanyFortrea is a leading global clinical research organization providing end-to-end clinical development and safety solutions, supporting pharmaceutical and biotechnology companies worldwide.

Roles & Responsibilities• Conduct regular field visits to doctors, dentists, clinics, and hospitals across assigned Mumbai territories• Promote and detail pharmaceutical products effectively to healthcare professionals• Build and maintain strong, long-term professional relationships with doctors, dentists, and key opinion leaders• Achieve and exceed assigned sales targets within the designated territory• Collect market intelligence, monitor competitor activities, and gather customer feedback• Maintain accurate daily activity reports using CRM and sales tracking tools• Manage assigned territories across Mumbai, including South Mumbai, Bandra, Andheri East & West, Goregaon–Malad, Kandivali–Borivali, Kurla, Ghatkopar, Powai, Mulund, and surrounding areasQualification• Graduation in Pharmacy (B.Pharm), Life Sciences, or a related disciplineExperience• Freshers with relevant educational background are welcome• 6 months to 2 years of experience in pharmaceutical or medical sales is preferred• Experience in the dental segment will be an added advantageSkills• Strong communication and interpersonal skills• Ability to work in a field-based sales role with extensive travel• Good territory management and organizational skills• Self-motivated, target-driven, and passionate about healthcare salesAbout the OrganizationHorizontal Talent specializes in connecting skilled professionals with growing organizations across healthcare and pharmaceutical sectors, offering opportunities for career growth in competitive and high-potential markets.

Roles & Responsibilities• Research, write, and edit high-quality clinical and regulatory documents including clinical study reports, study protocols, and data summaries• Act as primary author for complex clinical and program-level documents such as CSR, Protocol, ICF, IB, IND, and MAA• Provide senior-level scientific and regulatory review of routine and complex medical writing deliverables• Serve as lead writer, offering training, mentorship, and guidance to junior writers and cross-functional team members• Advise internal and external stakeholders on document development strategy, regulatory expectations, and industry best practices• Ensure compliance with quality standards, SOPs, and regulatory guidelines for all assigned documents• Develop, review, and implement best practices, methodologies, and process improvement initiatives• Manage and review performance metrics for assigned projects to ensure delivery excellence• Support program management activities including timelines, forecasts, budgets, and identification of out-of-scope work• Assist business development efforts through proposal content review, client presentations, and bid defense participation• Represent the medical writing function in project launch meetings, review meetings, and cross-functional discussionsQualification• Bachelor’s degree in a scientific or life sciences discipline or equivalent qualification• Advanced degree preferredExperience• Minimum 8+ years of regulatory medical writing experience• Strong hands-on experience authoring CSR, Protocol, ICF, IB, and other regulatory documents• Proven experience managing complex medical writing projects• Prior experience in pharmaceutical or CRO environment required• Submission document experience preferred• Medical writing certifications (AMWA, EMWA, RAC) advantageousSkills• In-depth knowledge of global and regional regulatory document development guidelines• Strong expertise in one or more specialty areas such as regulatory, submissions, therapeutic areas, or clinical development• Excellent data interpretation, scientific writing, editing, and proofreading skills• Strong project management and organizational capabilities• Advanced written, verbal, and presentation communication skills• Strong negotiation, decision-making, and problem-solving abilities• Ability to work independently with high accountability• Proven capability to mentor and lead junior medical writersAbout the CompanyThermo Fisher Scientific, through its PPD® clinical research services, is a global leader in contract research supporting pharmaceutical and biotechnology organizations across all phases of clinical development. Operating in more than 100 countries, the organization delivers high-quality scientific, regulatory, and operational expertise to accelerate the development of life-changing therapies while upholding the highest standards of integrity, innovation, and collaboration.

Roles and responsibilities:• Work collaboratively with the clinic and cross-functional teams to ensure excellent patient care and experience• Take ownership of patient treatment and represent the organization professionally• Continuously learn and develop clinically to excel as a physiotherapist• Participate in ongoing mentoring and training programs to enhance clinical skills, particularly as a Spine Specialist• Maintain accurate patient records and documentationQualification:• Bachelor of Physiotherapy (BPT) – candidates should have completed 6 months of internship• Master of Physiotherapy (MPT)Experience:• Freshers and experienced physiotherapists are welcome to apply• Prior experience in a clinical or patient-facing physiotherapy role is a plusSkills:• Strong clinical assessment and physiotherapy skills• Excellent communication and interpersonal abilities• Ability to work collaboratively with a team and follow structured clinical protocols• Commitment to continuous learning and professional developmentBenefits:• 1-month comprehensive training program as a Spine Specialist• 2-month ongoing mentoring for successful induction into the clinic system• Professional growth in a supportive, patient-focused environmentAbout the company:Qi Lifecare Pvt. Ltd., established in 2002, is a healthcare organization dedicated to bridging the gap between fitness and medicine. The company specializes in lifestyle management and spinal care, using a fact-based and precise approach to treat lifestyle diseases. Qi Lifecare integrates medical expertise with exercise and nutrition strategies to provide comprehensive patient care across multiple locations in Mumbai.

Roles and responsibilities:• Provide physiotherapy services with a patient-centric approach• Assess and treat patients for musculoskeletal (MSK) or pelvic floor conditions• Develop individualized treatment plans and track patient progress• Collaborate with clinic staff to ensure high-quality patient care• Educate patients on exercises and rehabilitation strategies• Maintain accurate patient records and documentationQualification:• Bachelor’s or Master’s degree in Physiotherapy• Knowledge of musculoskeletal therapy, pelvic floor therapy, and rehabilitation practices• Strong understanding of patient assessment and treatment planningExperience:• 0–3 years of experience; freshers are welcome to apply• Experience in pediatric, adult, or specialized physiotherapy is a plusSkills:• Strong communication and interpersonal skills• Passionate, empathetic, and committed to patient care• Ability to work collaboratively in a professional clinic environment• Eagerness to learn and adapt to new therapeutic methodologiesBenefits:• Opportunity to work in a premium clinic environment• Exposure to a range of specialized physiotherapy practices• Supportive team culture encouraging growth and learningWorking hours:• Full-time and part-time options available; flexible scheduling depending on patient loadAbout the company:World of Wellness, led by Dr. Ushma, is a Malad West clinic focused on holistic health and patient-centric physiotherapy care. The clinic emphasizes excellence in clinical practice combined with compassionate care, helping patients rediscover true health. The team includes specialists in musculoskeletal therapy, pelvic floor therapy, and other physiotherapy domains, creating a premium healing environment for both patients and professionals.

Roles & Responsibilities• Generate, revise, and maintain clinical and regulatory documents for Core Labs projects• Coordinate quality control reviews of documents and maintain complete audit trails of revisions and approvals• Collaborate with internal teams to ensure document accuracy, consistency, and compliance with applicable standards• Provide input on data analysis planning and assess its impact on clinical document outcomes• Support cross-functional teams by delivering high-quality documentation within defined timelines• Perform additional documentation-related duties as assigned to support project and organizational needsQualification• Master’s degree in a health, life sciences, or science-related disciplineExperience• Suitable for early to mid-level professionals with clinical documentation exposure• Experience in clinical research, CRO, or laboratory documentation preferredSkills• Strong written and verbal communication skills• Intermediate knowledge of medical terminology and clinical patient management• Ability to manage multiple documents and maintain version control• High attention to detail and quality standards• Ability to work collaboratively in a team-based office environmentAbout the CompanyMedpace is a full-service global clinical contract research organization providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. With operations across more than 40 countries and deep therapeutic expertise, Medpace supports the development of safe and effective medical therapies through a disciplined, science-driven approach.

Roles & Responsibilities• Plan, organise, and execute scientific field activities for Rare Blood Disorders with focus on Hemophilia• Conduct in-depth, balanced, and non-promotional scientific discussions with Key Opinion Leaders and healthcare professionals• Disseminate scientific evidence, clinical study data, and treatment guidelines relevant to hematology and hemophilia• Support healthcare professionals on diagnostic pathways and patient management journeys• Plan and deliver scientific meetings, lectures, and advisory interactions within the therapeutic area• Align scientific field activities with Sanofi’s medical and strategic objectives• Collaborate in speaker training programs when required• Gather medical insights on treatment trends and unmet needs and provide structured feedback to internal teams• Participate in cross-functional meetings with brand and medical teams to align activities• Maintain full compliance with ethics, integrity standards, Sanofi policies, and industry regulations• Build and sustain long-term peer relationships with KOLs and key stakeholders• Work with diagnostic coordination teams to resolve diagnostic, documentation, and supply chain queries• Record and report insights using approved internal systems and tools• Support evidence-generation activities including investigator-led and clinical data collection initiatives• Operate independently while collaborating closely with the Rare Blood Disorder Medical AdvisorQualification• Advanced degree in Medical or Scientific discipline (MBBS, MD preferred)Experience• Minimum 2–4 years of experience as a Medical Science Liaison or Scientific Advisor• Prior experience in Hematology or Hemophilia strongly preferred• Experience interacting with opinion leaders in rare or specialty disease areas desirableSkills• Strong scientific knowledge of rare blood disorders, coagulopathies, and bleeding disorders• Excellent strategic planning, prioritisation, and execution skills• Strong communication, critical thinking, and problem-solving abilities• Ability to manage complex KOL opinions while aligning with corporate medical strategy• Deep understanding of local pharmaceutical regulations and non-promotional compliance requirements• Capability to work cross-functionally and manage multiple stakeholders• Advanced proficiency in English (written and spoken)About the CompanySanofi is a global healthcare leader focused on discovering, developing, and delivering innovative medicines and vaccines across specialty care, general medicines, and rare diseases. Through its strong Medical Affairs presence in India and globally, Sanofi is committed to scientific excellence, ethical engagement, and improving outcomes for patients with complex and rare conditions, including hematological disorders.

Roles & Responsibilities• Provide end-to-end oversight of animal health clinical trials from study set-up to completion• Obtain comprehensive understanding of study protocols, objectives, timelines, and deliverables• Define roles and responsibilities of study personnel and ensure alignment across teams• Collaborate with sponsors to establish and manage projected study timelines• Oversee execution of study activities to ensure tasks are completed accurately and on time• Manage GCP-compliant late-phase clinical trials in animal health• Review and contribute to study protocols, amendments, and final study reports• Monitor study progress, risks, and issues, ensuring timely escalation and resolution• Work cross-functionally with internal teams and external stakeholders to support study delivery• Ensure high standards of data quality, compliance, and documentation throughout the trial lifecycleQualification• Degree in Life Sciences, Veterinary Sciences, Pharmacy, or related disciplineExperience• Minimum 8+ years of clinical trial management experience within a CRO or animal health pharmaceutical organization• Proven experience managing GCP-compliant late-phase animal health clinical trials• Hands-on experience in protocol development and final study report writingSkills• Strong clinical trial management and leadership skills• High attention to detail with strong analytical mindset• Excellent time management and multitasking ability• Strong communication and stakeholder management skills• Dependability, flexibility, and ability to work effectively in team environments• Customer-centric and solution-oriented approachAbout the CompanyArgenta is a global animal health contract research and contract development and manufacturing organization (CRO/CDMO) dedicated exclusively to improving the lives of animals. Founded in 2006, Argenta partners with animal health companies worldwide, providing end-to-end solutions from molecule to market, supported by a strong culture of teamwork, innovation, customer focus, and global collaboration.

Role & Responsibilities• Plan, prepare, and engage with Thought Leaders (Doctors) to exchange scientific, educational, and research-related information• Proactively and reactively disseminate, clarify, and educate on scientific data, study protocols, abstracts, and professional literature in line with local regulations• Respond to medical and scientific queries from Medical Societies related to assigned products• Organize, support, and participate in advisory board meetings• Attend congresses and conventions to network with healthcare professionals and gather competitive intelligence• Plan and coordinate scientific training and education sessions within the assigned therapeutic area or product• Identify, profile, segment, and engage Thought Leaders in alignment with the Medical Affairs plan• Contribute insights on Thought Leader interests and expertise to support internal medical strategy• Prepare and submit timely reports and track activities against agreed objectives• Provide additional external scientific support, training, and education as requiredQualification• Qualification in Natural Sciences OR Medical background (MD, MBBS, BAMS, BDS, MDS)Experience• Experience in Medical Affairs, Medical Science Liaison, or scientific engagement roles preferredSkills• Basic knowledge of the Diabetology therapy area and related molecules• Understanding of clinical trials, including study design and scientific rationale• Strong presentation, written, and verbal communication skills• Ability to work independently and collaboratively in a team environment• Strong internal and external stakeholder relationship-building skillsAbout the CompanyBayer is a global life science organization driven by the mission of achieving Health for all and Hunger for none. With a strong focus on innovation, scientific excellence, and sustainability, Bayer fosters a diverse and inclusive work environment while delivering meaningful impact across healthcare and agriculture worldwide.

Roles & Responsibilities• Collect, review, and process Adverse Event (AE) and Serious Adverse Event (SAE) reports• Perform case processing and data entry in safety databases such as Argus, ARISg, Oracle, or similar systems• Conduct literature searches and review scientific publications for safety-related information• Assist in signal detection, risk assessment, and safety trend analysis• Ensure compliance with ICH-GCP, ICH-E2B, and applicable regulatory guidelines• Support preparation and review of PSURs, PBRERs, and other regulatory safety documents• Maintain accurate, complete, and audit-ready pharmacovigilance documentation• Coordinate with Clinical, Regulatory, Quality, and other cross-functional teams• Follow SOPs, timelines, and quality standards for safety reportingQualification• Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, or related disciplineExperience• Freshers are eligible to apply• Internship or academic exposure to pharmacovigilance or clinical research is an advantageSkills• Basic understanding of pharmacovigilance concepts and safety reporting• Knowledge of ICH-GCP and global drug safety regulations• Strong attention to detail and documentation skills• Good written and verbal communication skills• Ability to work in a team-oriented and compliance-driven environment• Willingness to learn safety databases and PV workflowsAbout the OrganisationThe organization is a growing healthcare and life sciences company focused on ensuring patient safety and regulatory compliance through high-quality pharmacovigilance and drug safety services, offering strong learning and career development opportunities for fresh graduates.

Roles & Responsibilities• Provide medical and scientific leadership and technical advice to Business Units, Pharmacovigilance, Medical Information, and Clinical Research teams• Oversee Medical Affairs activities in assigned therapeutic areas in India and coordinate with Regional and Global Medical Affairs teams• Ensure appropriate medical scientific support and training for marketing and sales teams in collaboration with training functions• Maintain up-to-date product and development project knowledge through internal communications and scientific literature review• Review and approve promotional materials in line with global SOPs, local laws, and compliance standards• Monitor competitor medical marketing activities locally and globally• Support regulatory, PV/MI, and Clinical Research teams with medical scientific inputs• Deliver internal and external medical presentations including advisory boards, launch symposia, and scientific meetings• Build and maintain strong relationships with Thought Leaders, societies, and medical associations• Provide overall medical inputs to Integrated Brand Plans including scientific expertise, thought leader management, and speaker development• Lead and manage study development programs including local studies, NIS, and Investigator Initiated Research (IIR)• Act as local medical expert for Global Clinical Development, supporting site feasibility and trial-related medical queries• Represent Bayer in external regulatory meetings for assigned products and therapy areas• Respond accurately and transparently to external medical and scientific queries from physicians, regulators, and the public• Support local safety issue and crisis management activities and collaborate with headquarters safety teams• Review patient support programs and market research initiatives to ensure pharmacovigilance compliance• Ensure inspection readiness, risk management, and high-quality execution of NIS studies• Stay current with regulatory requirements and ensure highest standards of Pharmacovigilance and Medical Affairs complianceQualification• MBBS and MD from a recognized Medical UniversityExperience• 2–3 years of experience as a Medical Advisor in Cardiology• Experience in driving medical strategy for cardiology or related therapy areas preferred• Clinical trial management experience is desirableSkills• Deep disease area expertise and strong scientific acumen• Excellent presentation, teaching, and communication skills• Strong stakeholder engagement and thought leader management capabilities• Ability to translate medical data into practical insights for commercial teams• Strong organizational, analytical, and numerical skills• Strategic thinking, innovation mindset, and results-oriented approach• High ethical standards with strong compliance and safety focus• Proficiency in MS Office and willingness to travelAbout the CompanyBayer is a global life sciences organization driven by its mission of “Health for all, Hunger for none.” With strong capabilities across pharmaceuticals, consumer health, and crop science, Bayer is committed to advancing science to solve some of the world’s toughest challenges.

Roles & Responsibilities• Prepare and maintain patient appointment folders in coordination with MRD and support staff• Coordinate billing activities and map vouchers accurately with respective patient folders• Observe patients’ physical condition and emotional changes and report to registered nursing professionals• Assist in maintaining a safe, clean, and comfortable hospital environment using appropriate patient care practices• Identify potential safety and health hazards and assist in implementing infection control and disaster prevention measures• Support physical and diagnostic examinations as required• Coordinate with medical officers, nurses, and hospital attendants for patient care and palliative patient movement• Manage patient linen requirements and assist with patient mobility when needed• Call patients from waiting areas for consultations and assist with patient queries• Support data retrieval from investigations and referrals• Coordinate patient appointments for diagnostics, admissions, surgeries, follow-ups, and referrals• Manage consultant room coordination including equipment functionality and consumable availability• Act as a liaison between patients and hospital stakeholders to ensure smooth service delivery• Perform additional duties as assigned by the nurse in chargeQualification• BSc (mandatory) / B.Pharm• Additional qualification in computer applications preferredExperience• Freshers are eligible• Prior hospital coordination experience will be an added advantageSkills• Good communication and interpersonal skills• Basic computer proficiency and documentation skills• Ability to coordinate with multiple hospital departments• Patient-centric approach with attention to detail• Ability to work in an on-site hospital environmentAbout the CompanyHinduja Hospital is a leading multi-specialty tertiary care hospital in Mumbai, known for its excellence in patient care, clinical services, and ethical medical practices. The hospital is committed to delivering high-quality healthcare through advanced medical infrastructure, skilled professionals, and a patient-first approach, while continuously strengthening standards in safety, compassion, and clinical excellence.

Roles & Responsibilities• Lead and line-manage a team of Clinical Research Associates (CRAs) based in Navi Mumbai• Recruit, onboard, train, and continuously develop CRAs to meet organizational standards• Oversee and guide CRAs to ensure high-quality delivery of core clinical monitoring responsibilities• Conduct regular one-to-one coaching sessions and provide constructive performance feedback• Track and manage CRA resourcing, workload allocation, and assignment planning• Support CRA engagement, retention, and career development aligned with company objectives• Collaborate with regional and local operations and cross-functional teams• Work closely with senior leadership to build and scale the clinical monitoring team in India• Travel for on-site evaluation and support of CRAs as required (approximately 10%)Qualification• Bachelor’s degree or higher in Life Sciences or a related disciplineExperience• 1–2 years of experience as a line manager or• Minimum 4 years of clinical monitoring experience as a CRA with readiness to move into line management• Prior experience in a global CRO preferredSkills• Strong leadership, mentoring, and people management skills• Advanced knowledge of Good Clinical Practice (GCP)• Excellent written and verbal communication skills• Ability to motivate, engage, and develop clinical research professionals• Strong organizational and resource management skills• Willingness to travel for CRA evaluationsAbout the CompanyMedpace is a full-service global clinical contract research organization providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device companies.

Roles & Responsibilities• Perform medical review of clinical, spontaneous, solicited, and literature adverse event cases (ICSRs)• Assess seriousness, causality, labeling, and overall medical accuracy of safety cases• Review narratives, AE/SAE terms, suspect drugs, concomitant medications, laboratory data, and medical history• Ensure compliance with global and local regulatory guidelines and adherence to SOP timelines• Provide medical inputs and product-related guidance to Drug Safety teams• Generate, send, and track medical follow-up queries• Review and respond to case-related queries within safety databases• Support audits, internal reviews, and client discussions• Provide medical input for SUSARs and other critical safety casesQualification• MBBS or equivalent (mandatory)Experience• Minimum 3+ years of experience in Pharmacovigilance / Drug Safety• Prior experience in medical review of ICSRs preferredSkills• Strong medical and clinical knowledge• Solid understanding of Pharmacovigilance and Drug Safety processes• Good problem-solving and decision-making abilities• Proficiency with MS Office and safety databases• Excellent written and verbal communication skills• Ability to work effectively in a multi-disciplinary team• High attention to detail and self-motivationAbout the CompanyLatinum HR Solutions is a specialized recruitment and staffing firm serving the life sciences, pharmacovigilance, and healthcare sectors in India. The organization partners with leading global life sciences companies to connect qualified medical professionals with long-term, non-clinical career opportunities in drug safety, regulatory, and allied domains, maintaining a strong focus on quality, compliance, and professional growth.

Roles & Responsibilities• Provide medical and scientific expertise for the design, execution, and interpretation of clinical trials (Phases I–IV) in Dermatology and Venereology in India• Ensure medical oversight of ongoing clinical studies, including safety monitoring and data review, in compliance with GCP and CDSCO guidelines• Collaborate with global and local R&D and Clinical Development teams on clinical strategy and protocol development• Engage with Key Opinion Leaders (KOLs) and healthcare professionals to disseminate scientific information and gather market insights• Contribute to publication strategies and deliver scientific presentations of clinical trial data• Ensure all medical affairs activities comply with Indian regulatory requirements and internal company policiesQualification• Educational background in Dermatology (MD/DNB or equivalent)• Strong understanding of clinical research and regulatory requirements in IndiaExperience• 8 to 10 years of experience in Medical Affairs or Clinical Research• Prior experience in dermatology-focused clinical trials preferredSkills• Strong knowledge of GCP, CDSCO regulations, and clinical trial methodology• Excellent scientific communication and presentation skills• Ability to engage and manage KOL relationships effectively• Strong cross-functional collaboration and stakeholder management skills• Analytical mindset with attention to regulatory and compliance standardsAbout the CompanyHuman touch Consultancy is a specialized talent acquisition and consulting firm that partners with healthcare, pharmaceutical, and life sciences organizations across India. The firm focuses on delivering high-quality recruitment solutions by connecting experienced medical and scientific professionals with organizations committed to innovation, compliance, and excellence in patient care and research.

Roles & responsibilities:• Evaluate patients’ physical conditions and assess rehabilitation needs• Develop and implement tailored physiotherapy treatment plans• Conduct therapy sessions for pain management, sports injuries, and other conditions• Educate patients on exercises, posture correction, and recovery strategies• Monitor and document patient progress, maintaining accurate records• Collaborate with other healthcare professionals as needed• Ensure effective rehabilitation outcomes and maintain professional standardsQualifications:• Bachelor’s or Master’s degree in Physiotherapy or related field• Expertise in physiotherapy techniques, rehabilitation practices, and manual therapyExperience:• Experience in patient assessment, treatment plan development, and implementation• Experience in pain management and sports injury recovery is a plusSkills required:• Excellent communication and patient education skills• Ability to work collaboratively with a multidisciplinary team• Strong organizational and record-keeping abilitiesAbout the company:Rise Physiotherapy is a physiotherapy and wellness center founded in 2021, dedicated to delivering efficient rehabilitation services. The center focuses on helping clients recover from aches, pains, injuries, and disabilities while providing trustworthy and expert care, aiming to touch lives and spread smiles.

Roles & Responsibilities• Analyze market trends, competition, and conduct market research to identify opportunities, threats, and key business issues• Develop and execute marketing strategies for Anti-cold, ENT, and Antibiotics product portfolio• Design innovative and informative promotional campaigns to strengthen field force detailing effectiveness• Monitor and control marketing expenses to maximize return on investment (ROI)• Coordinate with field force and cross-functional teams to address product-related challenges• Undertake extensive field visits to assess market dynamics, strategy implementation, and competitor activity• Actively participate in annual operating plan development and execution• Support brand building initiatives to strengthen growth trajectory of flagship brands, including SINAREST®Qualification• B.Sc/ M.sc/ B.Pharm / M.Pharm / MBAExperience• 2–4 years of experience in pharmaceutical marketing (Acute segment preferred)Skills• Strong understanding of pharmaceutical marketing and brand management• Experience in product lifecycle management and promotional planning• Market analysis and competitor intelligence capabilities• Effective coordination and communication skills• Willingness to travel extensively for fieldworkAbout the OrganizationCentaur Laboratories Pvt. Ltd. is a well-established Indian pharmaceutical company known for its strong presence in acute therapy segments. With iconic brands and a focus on innovation and growth, the organization offers an excellent platform for marketing professionals to build impactful pharmaceutical brands.

Roles & Responsibilities:• Assist the dentist during clinical procedures• Manage front desk operations and patient coordination• Prepare the clinic for treatments and maintain cleanliness• Handle basic administrative tasks as required• Ensure smooth daily functioning of the clinicQualification:• Minimum educational qualification Experience:• Freshers are welcome to applySkills:• Basic communication skills• Ability to manage front desk responsibilities• Organized and responsible approach to work• Willingness to learn and support clinical tasksWorking Hours:• Monday to Saturday: 10:00 AM – 6:00 PM• Thursday: 10:00 AM – 10:00 PM• Sunday: Weekly offAbout the Company:Comfort Dental Clinic is a patient-focused dental practice located in Nalasopara, Mumbai. The clinic is dedicated to delivering quality dental care while maintaining a professional and supportive environment for both patients and staff.