Are you an experienced Pharmacovigilance (PV) professional looking for your next career opportunity? BioClinAarc Pvt Ltd is inviting applications from candidates with expertise in Pharmacovigilance, Medical Review (MR), and Periodic Safety Update Reports (PSUR). If you have hands-on experience in drug safety operations and regulatory safety reporting, this is an excellent opportunity to advance your career.

Professionals with strong pharmacovigilance knowledge and experience in medical review and PSUR preparation are encouraged to apply.

Job Details

Key Responsibilities

• Perform Pharmacovigilance activities in compliance with global regulatory guidelines.
• Conduct Medical Review (MR) of Individual Case Safety Reports (ICSRs).
• Prepare and review Periodic Safety Update Reports (PSURs).
• Ensure timely safety data processing and regulatory compliance.
• Collaborate with cross-functional teams for safety evaluations.
• Maintain high-quality documentation and pharmacovigilance records.
• Support drug safety reporting and risk management activities.

Qualifications

Candidates should have:

• Relevant experience in Pharmacovigilance (PV).
• Strong knowledge of Medical Review (MR).
• Experience preparing or reviewing Periodic Safety Update Reports (PSUR).
• Good understanding of global pharmacovigilance regulations and drug safety practices.
• Strong analytical and communication skills.

Why Join BioClinAarc?

• Opportunity to work in a professional Pharmacovigilance environment.
• Exposure to Medical Review and regulatory safety reporting.
• Career growth in Drug Safety and Pharmacovigilance.
• Work with experienced industry professionals.
• Enhance expertise in global pharmacovigilance processes.

How to Apply

Application Link

We are accepting CV till 5 pm today 11 July 2026