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Regional Medical Advisor

Abbott
Abbott
1+ years
Not Disclosed
10 Jan. 6, 2026
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

Job Title: Regional Medical Advisor
Location: Mumbai, India
Category: Medical & Clinical Affairs
Experience Required: Minimum 1 year

Company Overview:
We are a leading pharmaceutical organization dedicated to advancing healthcare and improving patient outcomes across India. We are seeking a skilled and experienced Medical Affairs professional to join our team as a Regional Medical Advisor in Mumbai.

Role Summary:
The Regional Medical Advisor is an experienced individual contributor who operates under limited supervision, applying subject matter expertise in Medical Affairs. The role involves planning, executing, and overseeing clinical research activities, providing strategic support to medical teams, and ensuring compliance with regulatory standards.

Key Responsibilities:

  • Lead and oversee clinical trials (Phases III & IV) for company products, ensuring adherence to protocols and timelines.

  • Contribute to the design, implementation, and execution of clinical research protocols, including recruitment of investigators and negotiation of study designs and costs.

  • Facilitate data collection, analysis, and preparation of final clinical study reports.

  • Monitor clinical trials to ensure compliance with regulatory guidelines and internal quality standards.

  • Participate in adverse event reporting and ensure safety monitoring across clinical programs.

  • Coordinate and oversee investigator initiations, site management, and group studies.

  • Serve as a consultant or liaison with partner organizations when working under licensing agreements.

  • Provide reporting and documentation for submissions to regulatory agencies.

Qualifications:

  • Associate’s degree (or equivalent, ~13 years of education) in a relevant field.

  • Minimum 1 year of experience in clinical research, medical affairs, or related pharmaceutical functions.

Skills and Competencies:

  • Strong understanding of clinical trial management and regulatory compliance.

  • Ability to coordinate and manage multiple stakeholders, including investigators, regulatory bodies, and internal teams.

  • Effective communication and documentation skills.

  • Analytical mindset and attention to detail.

  • Self-motivated with the ability to work independently and under limited supervision.

Why Join Us:
This position offers the opportunity to contribute directly to clinical research and medical affairs strategies within a leading pharmaceutical organization. You will play a key role in supporting clinical programs and advancing scientific knowledge across therapeutic areas in India.