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Regional Medical Advisor

Abbott
Abbott
1+ years
Not Disclosed
10 Dec. 15, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Regional Medical Advisor – Medical Affairs

Location: New Delhi, India
Category: Medical and Clinical Affairs
Employment Type: Full-Time
Experience Required: Minimum 1 year in clinical or medical affairs


About the Role

The Regional Medical Advisor is an experienced medical affairs professional who operates with limited supervision and applies subject matter expertise to support clinical, research, and regulatory objectives. This role involves planning, executing, and overseeing clinical trials, ensuring data integrity, and facilitating regulatory compliance. The advisor serves as a key link between clinical operations, investigators, and regulatory bodies, contributing to the successful development and evaluation of company products.


Key Responsibilities

  • Oversee and direct clinical trials and research activities, including Phase III and Phase IV studies.

  • Implement clinical protocols, monitor adherence, and ensure completion of study reports.

  • Recruit and manage clinical investigators, negotiating study design, timelines, and budgets.

  • Ensure adverse event reporting and safety monitoring in compliance with regulatory standards.

  • Provide accurate reporting and documentation for regulatory submissions.

  • Coordinate and oversee investigator initiations and multi-center studies.

  • Serve as a consultant or liaison under licensing agreements when applicable.

  • Collaborate with cross-functional teams including Regulatory Affairs, Medical Affairs, and R&D to support product development and post-market activities.


Required Qualifications

  • Associates Degree or equivalent in life sciences, pharmacy, medicine, or related field.

  • Minimum 1 year of experience in clinical research, medical affairs, or a related field.

  • Knowledge of clinical trial protocols, regulatory compliance, and safety monitoring.

  • Effective verbal and written communication skills.

  • Ability to work independently while managing multiple priorities.


Why Join

  • Contribute to clinical development and regulatory compliance for innovative healthcare products.

  • Gain exposure to cross-functional medical affairs operations in a global healthcare company.

  • Access professional development opportunities to advance your career in Medical and Clinical Affairs.

  • Work in a dynamic environment promoting collaboration, learning, and excellence.

Abbott is an Equal Opportunity Employer, committed to diversity and professional growth.

Apply Now to join as a Regional Medical Advisor and help shape clinical and medical strategies that improve patient outcomes.