Browse the latest opportunities in Mumbai.
Serve as a scientific peer-to-peer resource to disease experts and healthcare professionals. Must have PhD, PharmD, or MD. **Job Duties:** - Diagnose and treat patients. - Prescribe medications as necessary. - Order and interpret diagnostic tests. - Advise patients on preventative health. **Benefits:** - Health insurance. - Paid time off. - Continuing education support.
About the role & responsibilities • Act as CTMS subject matter expert and support system upgrades and user queries • Develop and maintain CTMS training materials and training matrix • Manage global trial disclosures and ensure regulatory compliance • Maintain eTMF systems as per DIA reference model and SOPs • Support LMS coordination and training documentation • Contribute to SOP review and quality compliance activities • Create dashboards and analytics using Power BI and BI tools • Perform data integrity and validation checks • Coordinate with internal and external stakeholders Qualification • Master’s in Science / Computers / Advanced Data Analytics • Equivalent industry experience accepted Experience • Minimum 5 years in pharma, IT software or data analytics domain Skills • CTMS, eTMF and Trial Disclosure management • Dashboard and BI analytics • SOP and compliance knowledge • MS Excel and MS Word proficiency • Strong documentation and multitasking skills About the company • Abbott Leading global pharmaceutical organization
About the role & responsibilities • Maintain complete and inspection-ready TMF • Review and approve TMF documents for quality and compliance • Manage version control and document consistency • Maintain eTMF system structure and health • Act as TMF point of contact during audits and inspections • Coordinate with CRAs for TMF updates • Conduct TMF gap analysis and process improvements Qualification • Bachelor’s / Master’s in Pharmacy, Life Sciences, Biology, Chemistry, Nursing or Public Health • PG Diploma in Clinical Research accepted Experience • 0–2 years • Freshers eligible Skills • eTMF management • Regulatory documentation knowledge • Audit and inspection readiness • MS Office and documentation tools • Strong communication skills About the company • Sun Pharmaceutical Industries Ltd is India’s largest pharmaceutical company with global operations
About the role & responsibilities • Maintain study documents including protocols, ICFs, CRFs and reports • Organize electronic and paper trial master files • Coordinate meetings, travel arrangements and minutes • Support regulatory document preparation and submissions • Ensure compliance with GCP and regulatory standards • Track site invoices and payments • Manage vendor code generation and vendor tracking Qualification • Bachelor’s / Master’s in Pharmacy, Life Sciences, Biology, Chemistry, Nursing or Public Health • PG Diploma in Clinical Research accepted Experience • 0–2 years • Freshers eligible Skills • Clinical documentation management • GCP and regulatory compliance knowledge • MS Office proficiency • Coordination and communication skills • High attention to detail About the company • Sun Pharmaceutical Industries Ltd is India’s largest pharmaceutical company with global operations
About the role & responsibilities • Review and contribute to Safety Data Exchange Agreements ensuring quality and compliance • Support preparation of licensing agreements within assigned therapeutic areas • Participate in internal project-focused medical safety meetings • Engage in external scientific and non-regulatory meetings with consultants and partners • Maintain audit and inspection readiness • Lead or support safety process improvement initiatives • Provide medical safety support for US and RoW case management functions • Review and approve investigator safety reports with Clinical Development physicians Qualification • MBBS / MD Experience • Minimum 3 years in signal management, safety report authoring and benefit–risk management planning Skills • Signal management • Safety report writing and review • Benefit–risk evaluation • Regulatory compliance understanding • Strong analytical and communication skills About the company • Tata Consultancy Services (TCS) is a global IT and digital transformation leader with strong life sciences and healthcare operations
About the role & responsibilities • Act as scientific ambassador for oncology portfolio • Engage with KOLs and healthcare professionals for peer-to-peer scientific exchange • Deliver balanced, evidence-based medical information • Conduct advisory boards, CMEs, and scientific roundtables • Implement country-level medical affairs plans aligned to global strategy • Generate actionable medical insights for lifecycle management • Support real-world evidence generation • Drive scientific support for oncology product launches • Train internal commercial and marketing teams on disease and product science • Collaborate with clinical development, regulatory, market access and commercial teams • Ensure compliance with ICH-GCP, SOPs and regulatory guidelines • Perform adverse event and product complaint reporting Qualification • MBBS / MD / PhD / equivalent advanced degree in life sciences Experience • Minimum 2+ years in medical affairs or MSL role in oncology Skills • Strong oncology and biomarker knowledge • Excellent scientific communication and presentation skills • KOL relationship building and stakeholder engagement • Clinical trial data interpretation • Strategic planning and analytical thinking • Proficiency in MS Office and CRM tools Location & territory • North India region About the company • A global research-driven biopharmaceutical organization focused on developing innovative medicines and vaccines that improve patient outcomes
About Role & Responsibilities • Serve as a scientific resource for healthcare professionals, providing expert knowledge on medical products and disease areas • Facilitate peer-to-peer scientific discussions with key opinion leaders (KOLs) • Support clinical research and assist in the development of medical strategies • Provide training and scientific support to internal teams and external stakeholders • Maintain a deep understanding of scientific advancements and regulatory requirements Qualification • PhD, PharmD, or MD Experience • 2+ years of experience in medical affairs or a related field Skills • Strong scientific knowledge and communication skills • Ability to engage with KOLs and healthcare professionals • Understanding of clinical data and regulatory requirements About the Company Novartis India is a leading global healthcare company focused on providing life-saving treatments and improving health worldwide
Serve as a scientific peer-to-peer resource to disease experts and healthcare professionals. Must have PhD, PharmD, or MD. **Job Duties:** - Diagnose and treat patients. - Prescribe medications as necessary. - Order and interpret diagnostic tests. - Advise patients on preventative health. **Benefits:** - Health insurance. - Paid time off. - Continuing education support.
Serve as a scientific peer-to-peer resource to disease experts and healthcare professionals. Must have PhD, PharmD, or MD. **Job Duties:** - Diagnose and treat patients. - Prescribe medications as necessary. - Order and interpret diagnostic tests. - Advise patients on preventative health. **Benefits:** - Health insurance. - Paid time off. - Continuing education support.
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.
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. **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.
About the role & responsibilities • Act as the primary scientific face of the organization for assigned therapy areas • Identify, map and engage key opinion leaders (KOLs) and thought leaders • Execute medical affairs strategy including medical education, advisory boards and evidence generation • Provide scientific discussions to HCPs on disease areas, products and treatment trends • Support patient outcomes through scientific communication and insight generation • Handle scientific queries from physicians and stakeholders • Conduct disease trend analysis and contribute to annual medical strategy planning • Collaborate on research activities, publications, case studies and real-world evidence generation • Train sales and marketing teams on scientific updates • Ensure compliance with COBE and regulatory guidelines • Support product pipeline development through unmet need identification Qualification • MBBS with full-time postgraduate qualification (minimum 2 years) in any medical discipline • OR MBBS with MBA from a reputed institute Experience • Fresh postgraduates or up to 2 years experience in field-based medical affairs Skills • Strong scientific and research knowledge • Medical data interpretation and communication • KOL engagement and relationship building • Strategic thinking and analytical skills • Presentation and training capabilities • Excellent interpersonal and communication skills • Compliance and ethics awareness About the company • Dr. Reddy’s Laboratories is a leading multinational pharmaceutical company operating in 66+ countries, committed to affordable and innovative medicines with a strong focus on science, sustainability and patient access
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.
About the Company • MSD is a global biopharmaceutical leader focused on innovative medicines, vaccines, and oncology research • Strong presence in Medical Affairs, clinical research, and global regulatory compliance About the Role & Responsibilities • Act as scientific ambassador for oncology therapeutic portfolio • Engage Key Opinion Leaders (KOLs) for scientific exchange and relationship building • Support medical affairs strategy planning and execution • Conduct CMEs, advisory board meetings, and scientific discussions • Provide medical and scientific inputs to internal stakeholders • Support real-world evidence generation and publication initiatives Qualification • MBBS / MD / PhD (Life Sciences) Skills • Strong oncology domain knowledge • Excellent scientific communication and presentation skills • KOL engagement and stakeholder management • Medical strategy understanding • Good documentation and reporting Experience • 2+ years of experience in Medical Affairs / Medical Science Liaison (oncology preferred) Salary • Competitive salary package Benefits • Global oncology project exposure • Career growth and leadership opportunities • Continuous learning and professional development
Serve as a scientific peer-to-peer resource to disease experts and healthcare professionals. Must have PhD, PharmD, or MD. **Job Duties:** - Diagnose and treat patients. - Prescribe medications as necessary. - Order and interpret diagnostic tests. - Advise patients on preventative health. **Benefits:** - Health insurance. - Paid time off. - Continuing education support.
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.