Medical Reviewer - Trainee Freshers Job at Sitero | 8 - 12 LPA

Sitero, a leading clinical research and life sciences organization, is hiring a Medical Reviewer – Trainee for its Drug Safetyteam in Mysuru (Hybrid). This role is ideal for medical graduates (MBBS or higher) with0-1 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 tosafety 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?

Application Link

By Admin

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