Sitero, a leading clinical research and life sciences organization, is hiring a Medical Reviewer – Trainee for its Drug Safety team in Mysuru (Hybrid). This role is ideal for medical graduates (MBBS or higher) with 0-1 years of experience in Drug Safety and Pharmacovigilance (PV). The position offers a competitive salary (8-12 LPA), variable pay, healthcare benefits, and career growth opportunities in a dynamic clinical research environment.
📍 Location: Mysuru (Hybrid)
💰 Salary: 8-12 LPA
📅 Experience: 0-1 years (Clinical Practice) | 1+ year (PV preferred)
🎓 Qualification: MBBS or higher
📌 Job Type: Full-time, Permanent
About Sitero
Sitero is a global leader in clinical research services and software solutions for the life sciences industry. With expertise across early-phase to Phase III trials, Sitero provides technology-driven clinical solutions ensuring compliance, ethics, and innovation. The company specializes in drug safety, pharmacovigilance, and risk management, supporting pharmaceutical and biotech firms worldwide.
Why Join Sitero?
✔ Competitive salary & variable pay
✔ Paid time off & healthcare benefits
✔ Retirement benefits
✔ Hybrid work flexibility
✔ Career growth in global pharmacovigilance
Job Description: Medical Reviewer – Trainee
Key Responsibilities
- Analyze and interpret safety data from clinical trials, spontaneous reports, and literature.
- Perform medical review of Individual Case Safety Reports (ICSRs) including causality assessment.
- Contribute to safety reports (DSURs, PBRERs) and regulatory compliance.
- Support risk management and signal detection activities.
- Assist in SOP development, training programs, and investigator meetings.
- Collaborate with Regulatory Affairs for pharmacovigilance compliance.
- Mentor Pharmacovigilance Specialists and ensure adherence to ICH, CIOMS, FDA, EMA guidelines.
Skills & Qualifications
✅ MBBS or higher medical degree (required).
✅ 0-1 years in clinical practice (mandatory).
✅ 1+ year in Drug Safety/Pharmacovigilance (preferred).
✅ Knowledge of US/EU PV regulations, ICH-GCP, CIOMS.
✅ Experience in ICSR medical review, coding (MedDRA), and benefit-risk assessment.
✅ Strong analytical, communication, and presentation skills.
How to Apply?
