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Safety & Pv Intern/Trainee – Pharmacovigilance Internship

Syneos Health
Syneos Health
0 years
Not Disclosed
Hyderabad
3 May 11, 2026
Job Description
Job Type: Internship Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

Safety & PV Intern/Trainee – Pharmacovigilance Internship Opportunity

Company: Syneos Health
Job Title: Safety & PV Intern/Trainee
Location: Hyderabad, India
Work Mode: Office-Based
Job Type: Contractual Internship / Trainee Role
Duration: 1 Year (Performance-Based Continuation)
Job ID: 25106348


About the Opportunity

Syneos Health is hiring Safety & PV Interns/Trainees for its Hyderabad office. This opportunity is ideal for fresh graduates and recent pass-outs interested in building a career in Pharmacovigilance, Drug Safety, Clinical Safety Operations, and ICSR Processing.

The selected candidates will gain hands-on exposure to global pharmacovigilance processes, safety databases, case handling, MedDRA coding, literature screening, safety reporting, and regulatory compliance activities within a leading global life sciences organization.

This role is specifically designed for freshers and 2024–2025 pass-out candidates from healthcare and pharmacy backgrounds.


Key Responsibilities

Pharmacovigilance & Safety Operations

  • Monitor and route incoming safety information to appropriate project teams
  • Record and track ICSR documentation according to sponsor and company guidelines
  • Assist in case creation and safety database entry
  • Ensure proper case processing conventions and compliance standards are followed
  • Support query follow-up and workflow reconciliation activities

Drug Safety & Case Processing Support

  • Assist with:
    • MedDRA coding
    • Drug coding
    • Narrative writing
    • Coding of adverse events and medical history
    • Concomitant medication and test coding
  • Support duplicate ICSR identification and management
  • Participate in expedited safety reporting activities
  • Assist with safety literature screening and review

Regulatory & Documentation Activities

  • Support submission processes and safety documentation management
  • Maintain Trial Master File (TMF) and Pharmacovigilance System Master File documentation
  • Ensure compliance with:
    • ICH Guidelines
    • GCP
    • GVP Modules
    • Regulatory safety reporting requirements
  • Participate in audits and quality-related activities when required

Data Management & Compliance

  • Redact patient-identifying information in compliance with data privacy regulations
  • Manage translation workflows for safety source documents
  • Support xEVMPD product validation and SPOR/IDMP-related activities
  • Maintain documentation accuracy and regulatory traceability

Educational Qualification & Eligibility

Candidates must belong to one of the following educational backgrounds:

  • M.Pharm
  • Pharm.D
  • B.Pharm + MSc
  • BHMS
  • BDS
  • Ph.D. (Pharmacy)

Eligible Pass-Out Years

  • 2025 Pass-Outs
  • 2024 Pass-Outs with strong interest in Pharmacovigilance

Experience Required

  • Freshers are eligible to apply
  • No prior Pharmacovigilance experience required
  • Strong interest in Drug Safety and Clinical Safety Operations preferred