Regional Medical Advisor – Mumbai, India
Experience: Minimum 1 Year | Location: Mumbai, India | Category: Medical & Clinical Affairs | Employment Type: Full-Time
Company Overview:
Join a leading pharmaceutical organization dedicated to advancing healthcare through scientific excellence and innovative medical solutions. We are seeking a Regional Medical Advisor to contribute to our Medical Affairs team, supporting clinical research, trial management, and regulatory compliance in India.
Role Overview:
As a Regional Medical Advisor, you will be an experienced professional individual contributor working under limited supervision. This role requires applying medical and clinical expertise to support clinical trials, research initiatives, and regulatory reporting, ensuring adherence to protocols and high-quality outcomes.
Key Responsibilities:
Provide subject matter expertise within the Medical Affairs function, guiding planning, execution, and oversight of clinical trials and research activities.
Support the implementation of clinical protocols and facilitate completion of study reports.
Recruit clinical investigators and negotiate study designs, budgets, and timelines.
Direct and oversee human clinical trials (Phase III & IV) for products under development.
Participate in adverse event reporting, safety monitoring, and regulatory compliance activities.
Coordinate and provide accurate reporting information for submissions to regulatory authorities.
Monitor adherence to protocols, evaluate study completion, and ensure high-quality trial execution.
Coordinate investigator initiations, multi-site studies, and group collaborations.
Act as a consultant or liaison with partner corporations in licensing or collaborative agreements when required.
Qualifications:
Education: Associate’s Degree (± 13 years) or equivalent in a relevant medical or life sciences field.
Experience: Minimum 1 year in medical affairs, clinical research, or pharmaceutical/biotech environment.
Key Skills:
Strong knowledge of clinical trial design, execution, and reporting.
Understanding of regulatory and safety compliance requirements.
Excellent communication, negotiation, and stakeholder management skills.
Ability to work independently and make informed decisions under limited supervision.
Why Join Us:
Engage in cutting-edge clinical research and medical affairs initiatives.
Gain exposure to global standards in regulatory compliance, trial management, and pharmacovigilance.
Collaborate with a diverse and inclusive team of healthcare professionals.
Professional growth opportunities within a dynamic, innovation-driven environment.
Apply Now: Advance your medical affairs career as a Regional Medical Advisor and contribute to innovative healthcare solutions impacting patients globally.
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