Job Title: Safety & Pharmacovigilance (PV) Trainee – Freshers | Delhi NCR
Location: Gurugram, India
Job Type: Contract (1 Year)
Job ID: 25102900
Updated On: November 13, 2025
Syneos Health is a leading global biopharmaceutical solutions organization delivering integrated clinical, medical affairs, and commercial services. With operations across more than 110 countries and a workforce of over 29,000 professionals, Syneos Health focuses on accelerating the development and delivery of life-changing therapies.
This opportunity is designed specifically for fresh graduates from Delhi NCR seeking to start their career in Safety and Pharmacovigilance within a structured, growth-driven environment.
The Safety & PV Trainee will support end-to-end case processing activities, literature screening, medical coding, data entry, safety tracking, and regulatory documentation under the guidance of senior PV professionals. The role involves working within global SOPs, GVP, GCP, and ICH guidelines to ensure the accurate and compliant management of safety data.
Freshers only (0–1 year of experience)
Candidates must have passed out in 2025
Applicants must hold one of the following qualifications:
M.Pharm
Pharm.D
M.Sc + B.Pharm
BHMS
BDS
Ph.D. (Pharmacy)
Enter safety data into PV quality and tracking systems for ICSR receipt and documentation.
Assist in processing ICSRs in accordance with SOPs and study-specific safety plans.
Perform triage, completeness checks, accuracy verification, and regulatory assessment of ICSRs.
Conduct MedDRA coding for events, medical history, tests, and concomitant medications.
Prepare narrative summaries and identify follow-up requirements.
Support in the timely submission of expedited safety reports as per regulatory timelines.
Maintain safety activity trackers and documentation.
Perform literature screening, drug coding, and dictionary maintenance.
Manage xEVMPD product record validation and submission.
Identify and handle duplicate ICSRs.
Support SPOR/IDMP-related activities.
Ensure quality review of safety reports.
Upload required documentation to TMF or PSMF as per SOPs.
Maintain compliance with GCP, GVP, ICH guidelines, global regulations, and project-specific requirements.
Collaborate with cross-functional teams and participate in audits where required.
Apply updated regulatory intelligence to all safety reporting activities.
Strong scientific or healthcare knowledge base.
Proficiency in Microsoft Office and Outlook.
Excellent communication (written and verbal).
High accuracy with strong attention to detail.
Strong organizational capability and ability to work on multiple tasks.
Team collaboration and documentation skills.
Familiarity with safety databases and pharmacovigilance processes.
Understanding of medical terminology and pharmacology.
Working knowledge of Visio, Team Share, or equivalent collaboration tools.
This is a 1-year contractual position.
Extension will depend on performance and business requirements.
Syneos Health promotes career growth, continuous learning, and an inclusive culture that values diverse backgrounds and perspectives. The company offers technical and therapeutic training, performance-based progression, and a collaborative environment focused on impactful work in the biopharmaceutical industry.
Over the last five years, Syneos Health has collaborated on:
94% of all FDA-approved novel drugs
95% of EMA-authorized products
More than 200 clinical studies across 73,000 sites and over 675,000 patients
For more information, visit the official website:
syneoshealth.com
Interested candidates can apply directly through The Pharma Daily – Global Pharma Jobs Portal or join the Syneos Health Talent Network to receive updates on future opportunities.
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