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Medical Advisor

Abbott
Abbott
1-3 years
Not Disclosed
Mumbai, India
10 March 3, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Medical Advisor

Location: Mumbai, Maharashtra, India
Function: Medical and Clinical Affairs
Employment Type: Full-Time

Company Overview
Abbott Laboratories is a global healthcare organization dedicated to advancing science through innovative medicines and evidence-based medical engagement. With a strong presence in India, Abbott supports clinical excellence and regulatory compliance across therapeutic areas.

Role Overview
The Medical Advisor is an experienced individual contributor within the Medical Affairs function, working under limited supervision. This role requires strong subject matter expertise to support clinical research, protocol execution, investigator engagement, and regulatory compliance for company products.

This opportunity is well-suited for professionals seeking Medical Advisor jobs in Mumbai within a structured pharmaceutical Medical Affairs environment.

Key Responsibilities

Clinical Trial Oversight & Execution

  • Provide medical oversight for planning, execution, and monitoring of Phase III and Phase IV clinical trials.

  • Support implementation of approved clinical protocols and ensure timely completion of final study reports.

  • Monitor adherence to study protocols and ensure compliance with Good Clinical Practice (GCP) guidelines.

  • Coordinate investigator site initiations and manage collaborative group studies.

Investigator & Stakeholder Engagement

  • Recruit clinical investigators and negotiate study design and associated costs.

  • Serve as a medical consultant or liaison during licensing or collaborative agreements.

  • Engage with key opinion leaders (KOLs) to support scientific exchange and evidence generation.

Regulatory & Safety Responsibilities

  • Participate in adverse event (AE) reporting and pharmacovigilance monitoring.

  • Coordinate preparation of data and documentation for submission to regulatory authorities.

  • Ensure compliance with local regulatory requirements and company SOPs.

Scientific Contribution

  • Contribute to data collection activities and medical review processes.

  • Provide medical insights aligned with therapeutic area strategies.

Educational Qualifications

  • Associate’s Degree or equivalent qualification in Life Sciences, Pharmacy, Medicine, or related discipline.

  • Bachelor’s degree or higher preferred.

Experience Required

  • Minimum 1–3 years of experience in Medical Affairs, Clinical Research, or Clinical Trial Management within the pharmaceutical industry.

  • Exposure to Phase III and IV clinical studies preferred.

  • Understanding of regulatory submissions, pharmacovigilance processes, and GCP compliance.

Core Competencies

  • Clinical research coordination and oversight

  • Regulatory compliance and safety reporting

  • Investigator relationship management

  • Strong analytical and documentation skills

  • Effective cross-functional collaboration

Why Join Abbott?

  • Opportunity to contribute to late-phase clinical research initiatives.

  • Exposure to regulatory engagement and scientific leadership activities.

  • Career advancement within Medical Affairs and Clinical Development.

SEO & GEO Keywords: Medical Advisor Jobs Mumbai, Medical Affairs Careers India, Clinical Trial Jobs Mumbai, Pharma Medical Advisor Maharashtra, Phase III Phase IV Clinical Research Jobs India, Abbott Medical Affairs Jobs Mumbai.

This role offers a strong platform for early-to-mid-career medical affairs professionals seeking Medical Advisor positions in Mumbai with responsibilities spanning clinical trials, regulatory coordination, and scientific engagement within a leading global healthcare organization.