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Senior Medical Safety Physician - Cspv

Soterius
4-8 years
₹18 LPA – ₹35 LPA
Remote, India, 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, medical qualifications, and organization. Actual salary may vary.)

Job Summary

The Senior Medical Safety Physician is responsible for providing medical leadership in pharmacovigilance activities, including medical review of aggregate safety reports, signal management, benefit-risk assessment, regulatory safety documentation, and risk management planning. The role supports global safety surveillance by ensuring compliance with regulatory requirements and contributing to product safety evaluations throughout the product lifecycle.

Key Responsibilities

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

  • Screen and evaluate scientific literature for periodic safety reporting and regulatory submissions.

  • Provide medical assessment and scientific input for aggregate reports and Health Authority (HA) responses related to safety topics.

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

  • Ensure timely review, approval, and communication of signal management findings through safety 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 medical and scientific evaluations.

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

  • Lead the authoring and maintenance of Risk Management Plans (RMPs).

  • Collaborate with Safety Scientists, Medical Affairs, and Regulatory Affairs teams to implement safety strategies and risk minimization measures.

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

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

  • Ensure adherence to project guidelines, pharmacovigilance regulations, and quality standards.

  • Stay updated on new and evolving global pharmacovigilance regulations and regulatory requirements.

  • Train and mentor new team members in aggregate report writing and pharmacovigilance activities, when required.

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

  • Undertake additional responsibilities assigned by management.

  • Build and maintain strong collaborative relationships with cross-functional teams and global affiliates.

Required Qualifications

  • MBBS, MD, or an equivalent recognized Medical Degree.

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

  • Experience in medical review of aggregate safety reports and regulatory safety documentation.

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

Required Skills

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

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

  • Familiarity with ICH Guidelines, GVP Modules, and global pharmacovigilance regulations.

  • Experience preparing medical assessments and responding to Health Authority safety queries.

  • Excellent scientific review, medical writing, and analytical skills.

  • Strong communication and cross-functional collaboration abilities.

  • Ability to manage multiple projects and meet strict 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 activities.

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

  • Experience authoring Risk Management Plans (RMPs) and aggregate safety reports.

  • Ability to mentor teams and lead pharmacovigilance initiatives.

  • Familiarity with safety analytics, reporting, and data visualization tools.