Corporate Medical Job at Fortrea, Mumbai
Want to build a career in Pharmacovigilance and Medical Safety? If you are an MBBS, MD, DO, or an equivalent medical graduate looking to transition into the pharmaceutical industry, this opportunity at Fortrea could be an excellent choice. The company is hiring an Associate Medical Manager I to support post-marketing drug safety activities and medical review. This Corporate Medical Job in Mumbai offers exposure to pharmacovigilance, signal detection, aggregate safety reporting, and client interactions while working with a global clinical research organization.
About the Company:
Fortrea is a leading global contract research organization (CRO) dedicated to advancing clinical development and improving patient outcomes. The company provides end-to-end clinical research, pharmacovigilance, medical safety, and regulatory solutions to pharmaceutical, biotechnology, and medical device companies worldwide. With operations across multiple countries, Fortrea is committed to delivering high-quality scientific expertise, innovation, and regulatory excellence while supporting the development of safe and effective healthcare products.
Job Details:
- Job Title: Associate Medical Manager I
- Job Location: Mumbai, India
- Department: Medical Safety / Pharmacovigilance
- Employment Type: Full-Time
- Job Requisition ID: 263870
- Application Deadline: 17 July 2026
Key Responsibilities:
- Perform primary medical review of adverse event cases, including assessment of seriousness, causality, listedness/labeling, adverse event coding, and narrative review.
- Update and maintain daily case data and workflow trackers to ensure timely case processing in this Corporate Medical Job in Mumbai.
- Take complete ownership of assigned deliverables while meeting quality, compliance, productivity SLAs, and KPIs.
- Conduct secondary medical reviews (Quality Control) and retrospective reviews (Quality Assurance) to identify quality trends and improvement areas at Fortrea Careers.
- Provide medical guidance and training to the case processing team.
- Review aggregate safety reports, including PSURs, PADERs, and PBRERs.
- Participate in safety surveillance, signal detection, aggregate data review, and trend analysis.
- Attend and contribute to drug safety meetings and signal analysis discussions.
- Evaluate, interpret, and critically analyze safety data.
- Build effective working relationships with client medical teams and internal stakeholders.
- Mentor and coach medical writing teams to maintain quality and compliance standards.
- Conduct medical triage activities.
- Perform additional responsibilities assigned by the supervisor.
Educational Requirements for the Corporate Medical Job:
- Bachelor’s degree in Medical Science or
- MD, DO, or an equivalent medical degree.
- Equivalent relevant experience may be considered in place of educational qualifications, where applicable.
Skills Required:
- Strong knowledge of medical sciences, disease diagnosis, therapeutics, and drug treatments.
- Understanding of pharmacovigilance principles and medical safety.
- Knowledge of clinical research regulations.
- Good understanding of ICH-GCP guidelines.
- Familiarity with regulatory requirements related to Pharmacovigilance.
- Experience in medical case processing and medical review is preferred.
- Knowledge of signal detection and aggregate safety reporting.
- Excellent analytical and critical thinking skills.
- Strong written and verbal communication skills.
- Ability to mentor, train, and collaborate with cross-functional teams.
- Good organizational and time management skills.
Benefits of the Corporate Medical Job:
- Opportunity to work with a globally recognized Clinical Research Organization (CRO).
- Gain hands-on experience in pharmacovigilance and post-marketing medical safety.
- Exposure to aggregate safety reports, signal detection, and regulatory compliance.
- Collaborate with international pharmaceutical sponsors and medical experts.
- Enhance expertise in medical review and drug safety surveillance.
- Opportunity to mentor and guide pharmacovigilance professionals.
- Career growth in medical affairs, drug safety, and clinical research.
- Dynamic work environment focused on scientific excellence and continuous learning.
