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Senior Medical Safety Physician - Cspv

Soterius
4-8 years
₹18 LPA – ₹35 LPA
Greater Noida, Noida, India
15 Aug. 4, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

Senior Medical Safety Physician – Clinical Safety & Pharmacovigilance (CSPV)

Employment Type: Full-Time
Experience Required: 4–8 Years

Salary Package

Expected CTC: ₹18 LPA – ₹35 LPA (Estimated market range based on experience, organization, and therapeutic expertise. The original job description does not specify a salary.)

Job Summary

The Senior Medical Safety Physician is responsible for providing medical oversight for pharmacovigilance activities, including medical review of aggregate safety reports, signal management, risk management planning, and regulatory safety documentation. The role ensures compliance with global pharmacovigilance regulations while supporting product safety evaluation, benefit-risk assessment, and cross-functional collaboration.

Key Responsibilities

  • Perform medical review of aggregate safety reports, including PBRER, DSUR, and PADER, in accordance with global regulations and company SOPs.

  • Conduct scientific literature screening to support periodic safety reporting and regulatory submissions.

  • Lead product signal data review, analysis, and evaluation in collaboration with Product Leaders.

  • Ensure timely review, approval, and communication of safety findings through governance forums.

  • Contribute to safety governance meetings and participate in external meetings such as Data Monitoring Committees (DMC) and Adjudication Committees, where applicable.

  • Utilize safety data review, reporting, and visualization tools to support scientific and medical safety activities.

  • Review and contribute to the development of safety sections within regulatory documents.

  • Assume ownership of Risk Management Plan (RMP) authoring and maintenance.

  • Collaborate with Safety Scientists, Medical Affairs, and Regulatory Affairs teams on safety implementation and risk minimization strategies.

  • Provide medical and pharmacovigilance oversight for clinical protocols, Investigator Brochures, Safety Summaries, Clinical Study Reports, and periodic/ad hoc regulatory reports.

  • Develop, review, and implement Standard Operating Procedures (SOPs) and Work Instructions (WIs) while ensuring adherence to company and client procedures.

  • Ensure compliance with project requirements, regulatory guidelines, and pharmacovigilance standards.

  • Stay updated on new and revised global pharmacovigilance regulations.

  • Train and mentor new team members on aggregate report writing and pharmacovigilance processes, when required.

  • Perform administrative responsibilities related to project delivery and operational activities.

  • Carry out additional responsibilities assigned by management.

  • Build and maintain effective working relationships with cross-functional teams and global affiliates.

Required Qualifications

  • MBBS, MD, or an equivalent Medical Degree recognized by relevant medical authorities.

  • 4–8 years of experience in Pharmacovigilance, Clinical Safety, Drug Safety, or Medical Safety.

  • Strong experience in aggregate safety report authoring and medical review.

  • Sound understanding of global pharmacovigilance regulations and benefit-risk assessment.

Required Skills

  • Expertise in aggregate reports including PBRER, DSUR, PADER, and RMP.

  • Strong knowledge of signal detection, signal management, and benefit-risk evaluation.

  • Understanding of ICH guidelines, GVP Modules, and global regulatory requirements.

  • Experience in medical review of safety data and regulatory documents.

  • Strong analytical, medical writing, and scientific evaluation skills.

  • Excellent communication and cross-functional collaboration abilities.

  • Ability to manage multiple projects while meeting regulatory timelines.

  • Proficiency in pharmacovigilance databases, safety reporting tools, and Microsoft Office applications.

Preferred Skills

  • Experience with global regulatory submissions and health authority interactions.

  • Knowledge of clinical development and post-marketing pharmacovigilance processes.

  • Experience participating in Safety Governance Committees, Data Monitoring Committees (DMC), or Adjudication Committees.

  • Experience mentoring teams and leading pharmacovigilance initiatives.

  • Familiarity with data visualization and safety analytics tools.