Job Title: Regional Medical Advisor
Location: Mumbai, India
Category: Medical & Clinical Affairs
Industry: Pharmaceuticals / Healthcare
Experience Required: Minimum 1+ Year
Employment Type: Full-Time
The Regional Medical Advisor is a key individual contributor within the Medical Affairs function, responsible for providing scientific, clinical, and strategic medical support with limited supervision. This role requires strong subject-matter expertise in medical affairs, clinical research, and regulatory coordination, with the ability to apply scientific knowledge to region-specific business and compliance needs.
This position is well-suited for early-to-mid career medical affairs professionals seeking to build depth in clinical trials oversight, investigator engagement, and cross-functional collaboration within a regulated pharmaceutical environment.
Provide medical and scientific expertise to support Medical Affairs initiatives at a regional level.
Oversee the planning, direction, and execution of clinical trials, research activities, and data collection processes.
Support implementation of clinical study protocols and ensure timely completion of final clinical reports.
Direct and manage human clinical trials, particularly Phase III and Phase IV studies for products under development.
Recruit clinical investigators and collaborate on study design, feasibility, and cost negotiations.
Coordinate investigator site initiations, group studies, and ongoing study activities.
Monitor study progress, protocol adherence, and determine study completion milestones.
Participate in adverse event reporting and safety monitoring activities in line with regulatory and company guidelines.
Prepare, coordinate, and provide clinical and safety data for submissions to regulatory authorities.
Ensure compliance with applicable regulatory, ethical, and internal medical governance standards.
Act as a medical consultant or liaison when working under licensing or partnership agreements with external organizations.
Collaborate with internal stakeholders across clinical, regulatory, pharmacovigilance, and commercial teams to support aligned execution.
Associate Degree or higher in Life Sciences, Pharmacy, Medicine, or a related field
Advanced scientific or clinical qualifications are preferred and considered an advantage
Minimum 1 year of relevant experience in Medical Affairs, Clinical Research, Clinical Operations, or a related pharmaceutical role
Exposure to clinical trials, investigator coordination, or regulatory interactions is preferred
Strong understanding of Medical Affairs and clinical research processes
Knowledge of clinical trial phases, particularly Phase III and IV studies
Ability to interpret and apply clinical and scientific data
Understanding of pharmacovigilance and adverse event reporting
Strong coordination, documentation, and stakeholder management skills
Ability to work independently with limited supervision in a regulated environment
Why Join This Role
Opportunity to build a strong foundation in regional medical affairs and clinical research
Exposure to regulatory submissions, investigator management, and late-phase clinical trials
Career growth within a structured pharmaceutical and clinical governance framework
Gujarat :
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Canada |Quebec :
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Auckland |New Zealand :
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Madrid |Cebu Province :
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Croatia |Zagreb :
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Japan | Saitama |Tokyo :
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Kuala Lumpur |Kyiv Oblast :
Kyiv |Lima Region :
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South Africa | Midrand |Nišava District :
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