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Full-Time
Salary: 25k to 30k
Positions: 10

Pharmacovigilance Services Associate

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Safety Science Coordinator I

Full Time | Entry-Level | Office/Remote Option
Location: Pune, India
 Job ID: 255152
Posted: Today

End Date: October 31, 2025

About the Role

This position is ideal for candidates passionate about pharmacovigilance, clinical data management, and regulatory safety compliance—offering hands-on exposure to real-world safety operations within a global clinical research organization.

Role & Responsibilities

  • Assist in the processing and submission of Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs).

  • Maintain adverse event tracking systems, ensuring accuracy and completeness of records.

  • Support project setup and documentation, including creation of central study files and reporting templates.

  • Log and manage incoming Adverse Event (AE)/Serious Adverse Event (SAE) reports in departmental systems.

  • Perform data entry of safety data and ensure accurate MedDRA coding of adverse events.

  • Write patient narratives and assist in listedness assessments for marketed products.

  • Generate and track queries to collect missing or discrepant information.

Educational Qualification

  • Education:

    • Bachelor’s degree in Biological Sciences, Pharmacy, Nursing, Life Sciences, Medical Sciences, or a related field.

    • Advanced degrees (MS/MA/PharmD) preferred.

  • Experience:

    • 0–2 years of experience in Safety Operations, Pharmacovigilance, or Clinical Research.

    • Experience with AE/SAE processing, narrative writing, MedDRA coding, and safety database management preferred.

 

Location

 Pune, India

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