Pharmacovigilance Jobs | Manager Medical Review at Lambda
Discover rewarding pharmacovigilance jobs with Lambda Therapeutic Research, a global leader in clinical research. The Manager – Medical Review role in Ahmedabad offers exceptional opportunities for MBBS and MD professionals to contribute their medical expertise toward advancing drug safety and regulatory excellence. This position is ideal for experienced individuals passionate about ensuring quality and compliance in the medical review job domain while being part of an innovative and internationally recognized organization.
About the Company
Lambda Therapeutic Research Ltd. is a globally recognized Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With over 1500 employees across facilities in India, the UK, Poland, and the USA, Lambda delivers world-class pharmacovigilance and clinical research solutions to the biopharmaceutical and generic drug industries. Backed by 20+ years of experience, Lambda combines scientific innovation, technology, and quality systems to help clients bring safe and effective products to market efficiently.
Job Details:
- Job Role: Manager – Medical Review
- Req ID: 1398
- Location: Ahmedabad, India
- CTC Range: INR 11,00,000 – 20,00,000 per annum
Qualifications for this Pharmacovigilance Jobs
- MBBS or MD in a related discipline.
- 3–4 years of experience in pharmacovigilance (ICSR domain).
- Strong understanding of clinical data and regulatory compliance.
- Preferred: Experience in signal detection and aggregate report preparation.
Job Description
This medical review job involves overseeing the pharmacovigilance review of company, literature, and regulatory cases. The selected candidate will ensure clinical accuracy, proper coding, and detailed narrative evaluation in compliance with global safety standards. It’s an excellent opportunity for MBBS and MD professionals looking to advance their careers in pharmacovigilance jobs with an established global CRO.
Key Responsibilities for this Pharmacovigilance Jobs
- Conduct a comprehensive medical review of the company, literature, and regulatory cases.
- Select and evaluate adverse events with appropriate seriousness criteria.
- Perform MedDRA coding of adverse events accurately.
- Review reporter/company causality and perform label assessments.
- Identify product role (suspect, concomitant, or interacting).
- Evaluate concomitant conditions, medical history, and laboratory data.
- Prepare and assess detailed case narratives for accuracy and completeness.
