Mumbai Healthcare Jobs

Role & Responsibilities Plan, coordinate and oversee Phase III & IV human clinical trials Support implementation of clinical protocols and completion of final study reports Recruit clinical investigators and negotiate study design and budgets Coordinate investigator site initiations and multi-center studies Monitor protocol adherence and determine study completion Coordinate regulatory submissions and reporting to health authorities Participate in adverse event reporting and safety monitoring activities Collect, analyze and manage clinical research data Act as liaison with partner organizations under licensing or collaboration agreements Support clinical research planning and execution activities Qualification Associate Degree (or higher) in Life Sciences, Pharmacy, Nursing, Clinical Research or related discipline Experience Minimum 1 year of experience in Clinical Research / Medical Affairs / Clinical Trials Skills Clinical trial coordination Protocol compliance & monitoring Regulatory documentation and reporting Safety reporting knowledge Data collection & documentation Stakeholder coordination Basic project management skills About the Company A leading global healthcare organization engaged in advanced clinical research, medical affairs and post-marketing clinical development to support safe and effective therapeutic innovations.

Role & Responsibilities Build and maintain relationships with KOLs and HCPs in medical genetics, genomics, oncology, reproductive medicine and related specialties Present scientific and clinical data for genetics-based diagnostic products Act as primary scientific contact for product-related medical inquiries Support advisory boards, conferences, CMEs, and scientific symposia Deliver scientific training for internal sales, marketing and support teams Conduct educational programs and academic presentations for clinicians Support clinical trials, real-world evidence and post-marketing studies Provide test interpretation support and genotype-phenotype correlation guidance Collect medical insights from the field to support product and marketing strategy Ensure compliance with ethical, legal and regulatory standards Qualification PhD or MD in Medical Genetics, Molecular Biology, Genomics or related discipline Experience Relevant experience in medical affairs, clinical genetics, genomics or scientific liaison roles preferred Skills Scientific communication and presentation Clinical genomics knowledge KOL engagement and stakeholder management Strategic planning and insight generation Cross-functional collaboration Willingness to travel Pan-India About the Company HaystackAnalytics is a HealthTech genomics company backed by DST, BIRAC and DBT, developing advanced diagnostic solutions in infectious diseases and clinical genomics, including nationally recognized innovations in tuberculosis and personalized diagnostics.

Role & Responsibilities Lead product registrations and regulatory submissions including preparation of complex and routine filing packages Coordinate documentation, monitor timelines, and manage regulatory project activities Prepare responses to health authority deficiency letters Represent Regulatory CMC in cross-functional project meetings Monitor regulatory timelines and identify risks impacting project progression Maintain coordination with regional and affiliate regulatory teams Assess and approve lifecycle change requests and ensure ongoing compliance Develop Regulatory CMC strategies for assigned products and projects Identify and mitigate regulatory risks across product life-cycle Attend health authority meetings and provide licensing due diligence support Support process improvements, position papers, and regulatory work aids Maintain technical and regulatory knowledge of global and regional CMC requirements Qualification Bachelor’s degree in Pharmacy, Biology, Chemistry, Pharmacology, or related discipline Experience Minimum 10 years in Regulatory Affairs, R&D, Manufacturing, or related regulatory functions Skills Regulatory CMC strategy development Product registrations and lifecycle management Health authority interaction Risk management and compliance Cross-functional coordination Strong project management skills Technical regulatory documentation expertise Leadership, mentoring, and stakeholder management About the Company The organization is a global life sciences company engaged in pharmaceutical development and manufacturing, supporting worldwide regulatory compliance, product registration, and lifecycle management to deliver high-quality medicines to patients globally.

Role & Responsibilities • Execute Medical Affairs plan for AbbVie Oncology portfolio in India • Develop and maintain relationships with key opinion leaders, academic centers, and researchers • Provide scientific education and balanced medical information to healthcare professionals • Organize and support advisory boards, round tables, and scientific meetings • Present clinical and scientific data on AbbVie oncology products • Support clinical trials, research initiatives, and medical education programs • Serve as internal scientific resource for disease-state and product communications • Deliver ongoing training to medical affairs, sales, and cross-functional teams • Ensure compliance with regulatory, ethical, and company requirements • Maintain accurate documentation and manage activities within assigned budgets • Collaborate closely with Commercial, Medical Affairs, and R&D teams • Support HEOR, PV, and global medical office–related functions • High field engagement (approx. 60% travel) across assigned territories Qualification MD or MBBS Experience Minimum 2–3 years post-qualification experience in Medical Affairs Pharma industry or clinical research experience preferred Skills • Strong scientific communication and presentation skills • Ability to interpret and communicate clinical data effectively • Relationship building and stakeholder engagement • Cross-functional collaboration in matrix environments • Analytical thinking and problem-solving • Proficiency in MS Office tools About the Company AbbVie is a global biopharmaceutical leader focused on discovering and delivering innovative medicines across immunology, oncology, neuroscience, and eye care, with a strong commitment to improving patient outcomes worldwide

Role & Responsibilities • Perform medical review of clinical, solicited, spontaneous, and literature safety cases • Conduct medical assessment including seriousness, expectedness, labeling, and causality evaluation • Review and validate AE/SAE terms, suspect drugs, concomitant medications, lab data, and medical history • Ensure accurate narrative review and global coding consistency • Develop and maintain strong knowledge of disease biology and key safety concerns for marketed and investigational products • Ensure compliance with global regulatory requirements and internal SOP timelines Qualification • MBBS or equivalent medical qualification Experience • Experience in pharmacovigilance / medical review domain preferred Skills • Strong knowledge of PV regulations and safety case processing • Medical assessment and causality evaluation expertise • MedDRA coding and narrative review skills • High attention to detail and regulatory compliance awareness • Good communication and documentation skills About the Company TCS (Tata Consultancy Services) is a global IT services and consulting leader with a strong Life Sciences practice supporting pharmaceutical and healthcare organizations worldwide through advanced technology, analytics, and compliance-driven solutions.

Key Responsibilities Coordinate and monitor clinical trial activities from site start-up to close-out Perform on-site and remote monitoring visits in accordance with monitoring plans Conduct Risk-Based Quality Monitoring (RBQM), including SDV and SDR Review and manage data in EDC, CTMS, IWRS, and eTMF systems Ensure compliance with ICH-GCP, SOPs, and regulatory requirements Maintain audit readiness and support site audits and inspections Prepare monitoring visit reports and follow-up letters Track country-level site metrics and proactively resolve issues Maintain regular communication with investigators and site teams Support CAPA planning and implementation Mentor junior CRA team members when required Travel up to 60–75% as per monitoring plan Complete timesheets, expense reports, and other trial documentationEligibility Criteria Postgraduate degree in Life Sciences or related discipline Minimum 1–1.5 years of mandatory on-site monitoring experience Strong working knowledge of ICH-GCP and regulatory guidelines Experience in FSP model preferred Hands-on experience with EDC, CTMS, IWRS, and eTMF systems Valid driving license (where applicable) Excellent written and verbal communication skillsRequired Skills Stakeholder and site relationship management High attention to detail and documentation accuracy Ability to manage multiple studies simultaneously Strong problem-solving and risk mitigation capability Independent working with collaborative mindset Proficiency in MS Office and clinical trial softwareWhy Join CRG? Work on global trials across 100+ countries Exposure to Top-50 pharma and 750+ biotech sponsors Fully remote work model Clear career progression from CRA I to CRA II and senior levels Continuous training and mentoring programs Strong compliance-driven and quality-focused culture

Role & Responsibilities • Perform consultative selling of high-value treatment plans, programs and memberships at clinic reception • Manage clinic front desk operations and handle customer escalations professionally • Ensure timely inventory backfill of medicines and maintain clinic facility standards • Comply with SOPs to achieve and maintain clinic operations excellence certification • Manage doctor schedules and appointment flow • Track sales KPIs, perform root cause analysis and implement improvement plans • Ensure brand hygiene, dress code, grooming and service quality standards • Support smooth day-to-day clinic operations including weekend working Qualification • Graduate in any discipline preferred Experience • Proven experience in consultative face-to-face selling at clinics, centres or retail healthcare setups • Prior experience managing clinic or centre operations is mandatory Skills • Strong sales and negotiation skills • Customer handling and escalation management • Operational planning and inventory coordination • KPI tracking and performance analysis • Leadership, ownership mindset and problem-solving ability About the Role This role leads front-end clinic operations and consultative selling of high-value healthcare services, ensuring sales growth, service excellence, SOP compliance and superior patient experience while independently managing clinic operations.

Role & Responsibilities Update and maintain patient files during follow-up visits Record and maintain complete medical histories and patient information Perform daily OPD under the supervision of a senior doctor Assist senior doctors in primary consultation and clinical assessment Support prescribing of medications and provide OPD and IPD care Conduct clinical examination of couples and analyze investigation reports and test results Maintain accurate and clear medical documentation Assist doctors during sonography procedures Explain prescriptions and treatment plans to patients as per consultant’s advice Maintain IPD records, admission notes and discharge summaries Guide nursing staff for IPD patient care as per doctor’s guidelines Monitor medication administration and ward activities Qualification BAMS or BHMS Experience Minimum 2 years of relevant clinical experience Skills Clinical examination and patient assessment Medical documentation and record management Patient counseling and communication Basic sonography assistance Coordination with nursing staffAbout the Company Progenesis is a leading fertility healthcare organization dedicated to helping couples overcome infertility and achieve parenthood. Established in 2014, Progenesis provides compassionate, ethical and evidence-based fertility care and supports couples through every stage of their reproductive journey.

Role & Responsibilities Conduct post-discharge follow-up teleconsultations Monitor recovery progress and identify early warning signs Assess medication, laboratory, diet and physiotherapy adherence Provide evidence-based clinical guidance (non-prescribing) Escalate high-risk cases to the clinical team Educate patients on lifestyle modifications and self-care practices Coordinate referrals, diagnostic services and allied healthcare support Maintain accurate electronic medical records Collaborate with program managers to improve care delivery models Qualification MBBS (Mandatory) Additional certification in Family Medicine or Public Health is an advantage Experience 2–4 years of clinical practice preferred Family Medicine, Internal Medicine, Emergency or Community Health experience desirable Skills Strong clinical judgment and analytical ability Excellent communication and patient counselling skills Knowledge of post-hospitalization recovery protocols Ability to prevent readmissions through early intervention Familiarity with teleconsultation platforms preferred Benefits Fixed daytime working hours Permanent employment Exposure to digital healthcare and population health programs Career growth in HealthTech and Value-Based Care systemsAbout the Company HEAPS Health Solutions is a health-tech organization headquartered in Bangalore with offices in Mumbai, Hyderabad and Delhi. The company leverages data analytics, artificial intelligence and machine learning to deliver value-based digital healthcare and patient care coordination services.

Role & Responsibilities Conduct physiotherapy and aquatherapy assessments and treatments Manage assigned patient caseload independently Treat musculoskeletal, neurological and complex rehabilitation cases Plan, implement and review evidence-based rehabilitation programs Monitor progress and modify treatment plans for optimal outcomes Maintain accurate clinical documentation Participate in interdisciplinary assessment, treatment and discharge planning Educate patients, caregivers and relatives effectively Contribute to aquatherapy documentation, service development and research Assist in training therapy assistants and students Work independently with senior therapist support available Qualification Master’s in Physiotherapy (MPT) – Mandatory Experience Freshers may apply Skills Aquatherapy and rehabilitation techniques Clinical assessment and documentation Patient counselling and communication Evidence-based practice implementation Team coordination and independent working ability About the Company A specialised aquatherapy and rehabilitation centre delivering holistic, patient-centred care in a supportive and learning-focused clinical environment

Role & Responsibilities Oversee overall clinic operations and staff duties Manage clinical and non-clinical staff performance and responsibilities Develop and implement procedures for optimal patient care Handle hiring, training and performance evaluations Manage internal and external clinic communications Supervise daily operations including scheduling, records and workflows Ensure compliance with healthcare regulations and safety standards Manage budgeting, inventory and resolve patient concerns Design and implement business strategies to achieve organisational goals Monitor productivity, receivables and clinic performance metrics Develop and implement clinic protocols and SOPs Conduct quarterly and annual employee reviews Qualification Bachelor’s or Master’s degree in Physiotherapy Experience Minimum 10+ years of clinical and leadership experience Skills Strong leadership and team management skills Excellent communication and interpersonal abilities Problem-solving and decision-making skills Patient care management Organisational and multitasking abilities High attention to detail and regulatory compliance About the Company MPC is a growing healthcare organisation focused on delivering high-quality physiotherapy and rehabilitation services through structured clinical operations, professional leadership and patient-centred care

Role & Responsibilities Manage daily clinic operations and ensure smooth functioning Supervise physiotherapists and support staff Ensure high standards of patient care and clinical quality Oversee appointment scheduling, records and basic administration Handle patient concerns and maintain service excellence Qualification BPT or MPT Experience Minimum 5–10 years of clinical experience Prior experience in clinic or team management preferred Skills Strong leadership and team-handling skills Excellent patient communication and conflict handling Operational planning and clinic administration Decision-making and problem-solving ability About the Company A growing physiotherapy and rehabilitation clinic providing evidence-based patient care with a focus on quality outcomes, professional development and a collaborative working culture

About Role & Responsibilities • Perform pharmacovigilance activities such as signal detection and risk management • Ensure compliance with regulatory requirements for drug safety • Assist in preparing safety reports and presenting findings Qualification • B.Pharm Experience • 0-2 years in pharmacovigilance Skills • Strong understanding of pharmacovigilance processes • Good communication and report writing skills About the Company Cosette Pharma specializes in the development and commercialization of pharmaceutical products

Serve as a scientific peer-to-peer resource to disease experts and healthcare professionals. Must have PhD, PharmD, or MD. **What you will do:** - Lead daily clinical operations. - Mentor junior staff members. - Participate in quality improvement initiatives. **Requirements:** - Proven experience in the field. - Strong communication skills. - Valid license and registration.

Serve as a scientific peer-to-peer resource to disease experts and healthcare professionals. Must have PhD, PharmD, or MD. **Key Responsibilities:** - Provide high-quality patient care. - Collaborate with cross-functional teams. - Ensure compliance with medical standards. - Maintain accurate patient records. **About the Role:** This is a key position within our growing team. We offer competitive compensation and opportunities for professional development.

Serve as a scientific peer-to-peer resource to disease experts and healthcare professionals. Must have PhD, PharmD, or MD. **What you will do:** - Lead daily clinical operations. - Mentor junior staff members. - Participate in quality improvement initiatives. **Requirements:** - Proven experience in the field. - Strong communication skills. - Valid license and registration.

Key Responsibilities Act as scientific expert within franchise cross-functional teams Lead medical strategy, product ideation, evaluation, and regulatory scientific support Prepare SEC submissions, launch materials, CME and training content Review and approve promotional / non-promotional medical content Drive KOL engagement, advisory boards, medical education programs Support RWE studies, publications, and evidence generation Train sales and marketing teams on disease and product science Provide scientific responses to HCP and internal queries Represent Sun Pharma in internal and external scientific forums Eligibility & Experience MD Pharmacology 1–3 years experience as Medical Advisor / Sr. Medical Advisor Knowledge of ICH-GCP, Indian regulatory and ethics guidelines (MCI, UCPMP, DCGI) Strong research, scientific communication and medical writing skills Work Model Office-based (Mumbai) Travel: Less than 1 week per month

About Role & Responsibilities • Serve as a scientific peer-to-peer resource for disease experts and healthcare professionals • Engage in scientific discussions with key opinion leaders (KOLs) • Provide educational support and information on disease states and treatment modalities • Facilitate the exchange of scientific knowledge and research • Support the development of medical strategies Qualification • PhD, PharmD, or MD Experience • Experience in the pharmaceutical or medical industry preferred Skills • Strong scientific knowledge • Excellent communication and interpersonal skills • Ability to engage with KOLs and healthcare professionals Benefits • Health insurance • Paid time off • Continuing education support About the Company Novartis India is a global healthcare company that focuses on providing life-changing treatments across various therapeutic areas

About Role & Responsibilities • Monitor clinical trial sites for protocol compliance • Perform site initiation, monitoring and close-out visits • Ensure data quality and regulatory compliance • Coordinate with investigators and CRO teams • Maintain trial documentation and reports Qualification B.Pharm / M.Pharm / Pharm.D / MSc / BSc (Life Sciences) Experience 0 – 3 years Skills • GCP & ICH guidelines • Clinical monitoring • Documentation & reporting • Site coordination About the Company Thermo Fisher Scientific is a global leader in scientific services, clinical research and life-science solutions