Clinical Project Assistant
SanofiÂ
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Job Description
 Location: Bengaluru, India
Job No.: AIOC-S01608232
Employment Type: Full-time
Experience: 0–2 years
About the Role
We are currently seeking a Pharmacovigilance Services Associate to join our Life Sciences R&D vertical in Bengaluru. In this role, you will contribute to pharmacovigilance and drug safety surveillance, helping the world’s leading biopharma companies improve patient outcomes by connecting scientific expertise with meaningful insights into the patient experience.
Role & Responsibilities
- Manage Affiliate Mailbox and ensure accurate and timely reconciliation of safety reports as per process requirements.
- Perform written follow-up activities for both Serious and Non-serious Adverse Event (AE) cases.
- Handle case identification, data entry, MedDRA coding, case processing, and submission in compliance with client guidelines and regulatory requirements.
- Conduct follow-ups for Individual Case Safety Reports (ICSRs) in the safety database.
- Solve routine pharmacovigilance problems using established procedures and general guidelines.
- Collaborate with internal teams and supervisors for process improvements and issue resolution.
Educational Qualification
- Education: Bachelor of Pharmacy (B.Pharm) or equivalent degree in Life Sciences or related field.
- Experience: 0–2 years in Pharmacovigilance, Drug Safety, or Clinical Research.
- Skills & Competencies:
- Understanding of pharmacovigilance operations and global regulatory guidelines.
- Strong data entry accuracy, documentation, and analytical skills.
- Proficiency in MedDRA coding and pharmacovigilance databases (preferred).
- Good written and verbal communication abilities.
- Attention to detail and the ability to manage multiple tasks in a fast-paced environment.
- Understanding of pharmacovigilance operations and global regulatory guidelines.
Location
 Bengaluru, India
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