Safety & PV Trainee I Only for Freshers

Safety & Pharmacovigilance Trainee Freshers (Delhi NCR) Location: Gurugram, India Job ID: 25102900 Updated: 13 November 2025 Experience Required: 01 year (Freshers eligible) About the Opportunity Syneos Health is recruiting Safety & Pharmacovigilance Trainees for its Gurugram operations. This role is designed for fresh graduates seeking to begin their career in drug safety, ICSR processing, MedDRA coding, and global pharmacovigilance workflows. The position offers structured training, exposure to global regulatory requirements, and hands-on experience within a leading biopharmaceutical solutions organization. Key Responsibilities Enter ICSR details into PVG quality and tracking systems. Support case intake, triage, completeness check, and regulatory reportability assessment. Enter and validate data in global safety databases. Perform MedDRA coding of adverse events, medical history, investigations, and medications. Create accurate and comprehensive ICSR narrative summaries. Identify missing data, issue follow-up queries, and ensure timely resolution. Assist in preparing and submitting expedited regulatory safety reports. Maintain safety trackers, logs, and documentation as per guidelines. Conduct literature screening for safety insights and drug coding requirements. Support xEVMPD record maintenance and SPOR/IDMP-related activities. Identify and resolve duplicate ICSR entries. Perform quality review of processed cases. Ensure documents are filed in the Trial Master File or PV System Master File. Maintain compliance with SOPs, GCP, ICH, GVP, and global safety standards. Collaborate effectively with cross-functional teams and support audits when needed. Eligibility Criteria Education: M.Pharm, Pharm.D, B.Pharm, M.Sc (Life Sciences), BHMS, BDS, or Ph.D. (Pharmacy) Graduation Year: 2025 Experience Required: 01 year; freshers preferred Core Skills Strong foundation in life sciences or healthcare Excellent communication skills Proficiency in MS Office and Outlook High attention to detail and accuracy Strong documentation and multitasking abilities Ability to work effectively in team-based environments Preferred Skills Familiarity with pharmacovigilance, medical terminology, or safety databases Exposure to collaboration tools such as Visio or Team Share Additional Information This is a one-year contractual position, with continuation based on performance and business requirements. .