Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Pharmacovigilance Coordinator

Propharma
0-1 years
INR 3.5 LPA – 5.5 LPA
Remote, India, India
1 June 25, 2026
Job Description
Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

PHARMACOVIGILANCE COORDINATOR

Company: ProPharma
Location: India (Remote/Hybrid)
Department: Pharmacovigilance
Job Type: Full-Time


JOB OVERVIEW

The Pharmacovigilance Coordinator supports global drug safety operations by managing safety communications, performing case intake and book-in activities, conducting duplicate searches, supporting literature surveillance, entering safety data into pharmacovigilance databases, and ensuring accurate, timely processing of Individual Case Safety Reports (ICSRs) in compliance with regulatory requirements.


KEY RESPONSIBILITIES

Safety Case Intake & Coordination

  • Manage assigned pharmacovigilance mailboxes.

  • Perform inbox triage for:

    • Client communications

    • Incoming adverse event reports

    • Internal case processing requests.

  • Coordinate day-to-day pharmacovigilance workflow.

Case Processing Support

  • Perform duplicate searches.

  • Complete initial case book-in activities.

  • Enter basic safety data into pharmacovigilance databases.

  • Perform complete case data entry after appropriate training and qualification.

Literature & Regulatory Support

  • Support literature surveillance activities.

  • Conduct initial triage of regulatory authority database searches.

  • Assist with identification of potential safety cases from literature.

Data Management

  • Enter and maintain safety information including:

    • Patient details

    • Reporter information

    • Suspect products

    • Adverse events

  • Maintain accurate safety database records.

Privacy & Compliance

  • Screen and redact Protected Health Information (PHI) from source documents.

  • Ensure compliance with company procedures and pharmacovigilance regulations.

  • Maintain audit-ready documentation.

Client Communication

  • Prepare and send draft safety reports to clients for review.

  • Coordinate communications between internal teams and clients.

  • Support timely completion of client deliverables.

General Support

  • Assist with additional pharmacovigilance activities as assigned.

  • Support team operations and process improvements.


EDUCATIONAL QUALIFICATIONS

Required

  • Post-secondary education

Preferred

  • Bachelor's or Master's degree in:

    • Pharmacy

    • Life Sciences

    • Biomedical Sciences

    • Nursing

    • Biotechnology

    • Microbiology

    • Biochemistry


EXPERIENCE REQUIREMENTS

Required

  • Freshers may be considered

Preferred

  • 1+ year of Pharmacovigilance or pharmaceutical industry experience

Experience in:

  • Case Intake

  • ICSR Processing

  • Drug Safety

  • Safety Database Operations

  • Literature Screening