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

Safety & Pv Specialist I (Night Shift)

Syneos Health
2.5+ years
INR 5 LPA – 8 LPA
Gurgaon, India
1 June 11, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development

Safety & PV Specialist I (Night Shift)

Company: Syneos Health
Location: Gurugram, Haryana (Office-Based)
Employment Type: Full-Time
Shift: Night Shift (Mandatory)
Experience: Minimum 2.6 Years in Pharmacovigilance

About the Role

Syneos Health is hiring a Safety & PV Specialist I to support Pharmacovigilance operations, including ICSR processing, case management, medical coding, narrative writing, safety reporting, literature screening, and regulatory compliance activities. The role requires hands-on experience in drug safety and the ability to work in a night-shift environment.

Key Responsibilities

  • Process and manage Individual Case Safety Reports (ICSRs) as per SOPs and project requirements.

  • Review case information for completeness, accuracy, and regulatory reportability.

  • Enter and maintain case data in safety databases.

  • Perform coding of adverse events, medical history, concomitant medications, and laboratory tests using MedDRA.

  • Prepare complete and accurate case narratives.

  • Follow up on missing information and resolve case queries.

  • Support expedited safety reporting activities in compliance with regulatory requirements.

  • Conduct literature screening and safety review activities.

  • Maintain drug dictionaries and perform drug coding activities.

  • Support xEVMPD validation and submission activities.

  • Perform manual recoding of product and substance terms arising from ICSRs.

  • Identify and manage duplicate case reports.

  • Support SPOR / IDMP-related activities.

  • Conduct quality review of ICSRs.

  • Maintain Trial Master File (TMF) and Pharmacovigilance documentation.

  • Ensure compliance with GCP, GVP, ICH Guidelines, SOPs, and global safety regulations.

  • Participate in audits and inspection readiness activities.

  • Collaborate with internal and external stakeholders to support project deliverables.

Required Qualifications

Education:

  • B.Pharm

  • M.Pharm

  • BDS

  • BMS

  • MBBS

Not Eligible:

  • B.Sc

  • M.Sc

Experience:

  • Minimum 2.6 years of Pharmacovigilance experience.

  • Experience in ICSR Processing and Case Handling.

  • Exposure to MedDRA Coding and Safety Databases preferred.