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Medical Advisor - Mumbai

Abbott
Abbott
5-8+ years
Not Disclosed
Mumbai, India
10 March 19, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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 - Mumbai

Company: Abbott
Location: Mumbai, India
Job Type: Full-Time
Experience: Typically 5–8+ Years (Medical Affairs / Clinical Research)
Qualification: Not Specified
Salary Range: Not Specified

Job Overview

Abbott is hiring a Medical Advisor responsible for supporting medical affairs activities including clinical research, protocol execution, and stakeholder coordination.

The role involves overseeing clinical trials, contributing to medical strategy implementation, managing investigator relationships, and ensuring compliance with regulatory and safety requirements. The Medical Advisor will apply subject matter expertise to support data generation and clinical development activities.

Key Responsibilities

  1. Medical Affairs & Strategy

Support planning and execution of medical affairs initiatives.

Apply subject matter expertise to meet specific clinical and business needs.

Contribute to data generation and research activities.

  1. Clinical Trials Management

Oversee and manage Phase III and Phase IV clinical trials.

Support implementation of clinical protocols and ensure completion.

Facilitate preparation and finalization of clinical study reports.

  1. Investigator & Site Management

Recruit clinical investigators and manage relationships.

Negotiate study design and associated costs.

Coordinate investigator initiations and group studies.

  1. Safety & Pharmacovigilance

Participate in adverse event reporting and safety monitoring.

Ensure compliance with safety and reporting requirements.

  1. Regulatory & Reporting

Coordinate preparation and submission of reports to regulatory authorities.

Ensure adherence to clinical protocols and regulatory guidelines.

Monitor study progress and completion timelines.

  1. Stakeholder Collaboration

Act as liaison with internal teams and external partners.

Collaborate with external organizations under licensing agreements.

Support cross-functional coordination in clinical activities.

Required Skills

Medical Affairs Expertise

Strong understanding of medical affairs and clinical research.

Knowledge of clinical trial processes and data generation.

Clinical & Regulatory Knowledge

Understanding of regulatory requirements and reporting processes.

Familiarity with safety monitoring and adverse event reporting.

Analytical & Problem Solving

Ability to apply knowledge to solve complex problems.

Strong decision-making and analytical skills.

Communication & Collaboration

Effective stakeholder management and interpersonal skills.

Ability to work with cross-functional teams and investigators.

Operational Skills

Ability to manage multiple projects and timelines.

Strong organizational and execution skills.

Basic Qualifications

Relevant experience in medical affairs or clinical research

Experience in clinical trial management and investigator coordination

Preferred Competencies

Experience in Phase III and IV clinical trials

Strong regulatory and safety knowledge

Ability to work independently with limited supervision

Key Competencies

Medical affairs and clinical research execution

Clinical trial management and oversight

Regulatory compliance and reporting

Stakeholder and investigator management

Safety monitoring and pharmacovigilance

About the Company

Abbott is a global healthcare company focused on developing innovative products and technologies across diagnostics, medical devices, nutrition, and pharmaceuticals. The company is committed to improving health outcomes through science-based solutions and operates in over 160 countries worldwide.