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Associate Medical Manager 1

Fortrea
0-2 years
8 LPA - 15 LPA
Mumbai, India
1 June 22, 2026
Job Description
Job Type: Full Time Education: MBBS / MD / BDS / PharmD / B.Pharm / M.Pharm / B.Sc / M.Sc Skills: CPT, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, Medical Billing, Medical Coding

Associate Medical Manager – Pharmacovigilance / Drug Safety

Location: Mumbai, India
Company: Fortrea
Employment Type: Full-Time


Role Summary

The Associate Medical Manager is responsible for providing medical safety expertise and pharmacovigilance support for pharmaceutical, biotechnology, medical device, and combination product clients. The role involves medical review, signal detection, aggregate safety assessment, regulatory compliance, and safety data analysis in the post-marketing environment.

The position requires strong knowledge of medical sciences, clinical research, drug safety, and pharmacovigilance processes, while ensuring delivery of high-quality safety outputs in compliance with global regulatory requirements and client expectations.


Key Responsibilities

Medical Review & Safety Assessment

  • Perform aggregate medical review of safety data.

  • Evaluate adverse events and safety information for clinical significance.

  • Conduct medical assessment of safety cases and post-marketing reports.

  • Support benefit-risk evaluation activities.

Signal Detection & Safety Surveillance

  • Perform signal detection and signal analysis activities.

  • Identify emerging safety trends and potential risks.

  • Review aggregate safety data for signal validation and prioritization.

  • Support ongoing safety surveillance programs.

Pharmacovigilance Operations

  • Support post-marketing pharmacovigilance activities.

  • Maintain safety data quality and compliance standards.

  • Participate in case review and safety data evaluation.

  • Ensure timely completion of assigned deliverables.

Workflow & Data Management

  • Update and maintain case-related information in safety databases and tracking systems.

  • Document case feedback, safety assessments, and workflow activities.

  • Ensure accurate and timely maintenance of safety trackers and reports.

  • Support workflow management and productivity tracking.

Regulatory Compliance

  • Ensure compliance with:

    • Global Pharmacovigilance Regulations

    • ICH Guidelines

    • GCP Requirements

    • Client-Specific Procedures

  • Maintain inspection and audit readiness.

  • Adhere to internal SOPs and quality standards.

Client & Stakeholder Management

  • Support and strengthen client relationships.

  • Collaborate with global safety and medical teams.

  • Participate in client discussions and project meetings.

  • Deliver high-quality customer-focused support.

Quality & Process Improvement

  • Ensure deliverables meet defined quality standards and SLAs.

  • Participate in process improvement initiatives.

  • Contribute to operational excellence and compliance programs.

  • Support continuous improvement of pharmacovigilance processes.

Cross-Functional Collaboration

  • Work closely with:

    • Pharmacovigilance Teams

    • Medical Review Teams

    • Clinical Research Teams

    • Regulatory Affairs Teams

    • Quality Assurance Teams

  • Support project objectives and safety deliverables.


Required Qualifications

Education

  • Bachelor's Degree in Medical Sciences

OR

  • MD / DO or equivalent medical qualification


Experience

  • 0–2 years of experience in:

    • Pharmacovigilance

    • Drug Safety

    • Clinical Research

    • Medical Review

    • Clinical Practice

Preferred Experience

  • 1–2 years of pharmaceutical industry experience.

  • Experience in:

    • Case Processing

    • Medical Review

    • Safety Surveillance

    • Clinical Research Operations

  • 1–2 years of clinical practice experience preferred.