Trainee Job at Syneos Health | Freshers BPharm/MPharm/ Graduates Apply Now
Syneos Health is inviting fresh graduates from Delhi NCR to begin their career in Pharmacovigilance (PV) as a Safety & PV Trainee. This Trainee Job is designed for individuals passionate about healthcare, drug safety, and clinical research. As a trainee, you will gain hands-on experience in case processing, global safety regulations, medical coding, and PV quality systems—making it an ideal launchpad for a long-term career in drug safety and clinical operations.
- Job Post: Safety & PV Trainee
- Location: Delhi
About The Company
Syneos Health® is a fully integrated biopharmaceutical solutions organization, supporting clinical development and commercialization for global healthcare companies. With 29,000 employees across 110 countries, we work at the center of innovation to accelerate the delivery of life-changing therapies.
WORK HERE MATTERS EVERYWHERE — because every role contributes to better health outcomes worldwide.
Job Responsibilities
- Enter information into PVG quality and tracking systems for receipt and tracking ICSR as required.
- Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans as required.
- Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability.
- Enters data into safety database.
- Codes events, medical history, concomitant medications, and tests.
- Compiles complete narrative summaries.
- Identifies information to be queried and follows up until information is obtained and queries are satisfactorily resolved.
- Assists in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements.
- Maintains safety tracking for assigned activities.
- Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding as required.
- Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA.
- Manual recoding of un-recoded product and substance terms arises from ICSRs.
- Identification and management of duplicate ICSRs.
- Activities related to SPOR / IDMP.
- Quality review of ICSRs.
- Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post-marketing programs as appropriate.
Qualification Requirements for the Pharma Job
Education & Eligibility (Required)
- M.Pharm, Pharm.D, M.Sc + B.Pharm. , or Ph.D. (Pharmacy) passed out in the year 2025.
Core Skills (Required)
- Strong knowledge and interest in a healthcare/scientific background is a must.
- Proficiency in Microsoft Office Suite and Outlook.
- Strong organizational, documentation, and multitasking skills.
- Excellent written and verbal communication.
- Ability to collaborate effectively in a team environment.
- High attention to detail and accuracy.
Preferred Qualifications for the Pharma Job
- Familiarity with safety databases, medical terminology, pharmacology, or pharmacovigilance.
- Experience with collaboration tools (Visio, Team Share, or equivalent).
Important Note
This is a contractual role for a period of 1 year, with continuation subject to performance evaluation and business needs.
