Top Pharmacovigilance Jobs at Syneos Health | Apply Now
If you’re exploring rewarding Pharmacovigilance Jobs, the Safety & PV Specialist I role at Syneos Health offers a strong opportunity to begin or grow your journey in drug safety. As part of Syneos Careers, this position allows pharma professionals to contribute to global safety operations, ICSR processing, regulatory submissions, and end-to-end pharmacovigilance activities while working within one of the world’s leading biopharmaceutical solutions organizations.
Job Details:
- Job Title: Safety & PV Specialist I
- Remote Type: Office-based
- Locations: IND-Gurugram, IND-Hyderabad, IND-Pune
- Time Left to Apply: End Date: December 31, 2025 (30+ days left to apply)
- Job Requisition ID: 25102730
About The Company:
Pharmacovigilance Jobs at Syneos Health are part of a global mission to accelerate biopharmaceutical innovation. Syneos Health® is a fully integrated biopharmaceutical solutions organization that combines clinical, medical, and commercial expertise to support customers worldwide. Through Syneos Careers, the company empowers professionals to grow within a diverse, collaborative, and patient-centric environment spanning 110+ countries with over 29,000 employees.
Job Description | Pharmacovigilance Jobs
The Safety & PV Specialist I role supports global pharmacovigilance operations by processing ICSRs, ensuring regulatory compliance, maintaining safety databases, conducting literature reviews, supporting xEVMPD submissions, and contributing to both clinical and post-marketing safety activities. This position places candidates within one of the most impactful Pharmacovigilance Jobs available through Syneos Careers.
Key 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 reportability.
- 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.
- Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, GVP, project/program plans and the drug development process.
- Fosters constructive and professional working relationships with all project team members, internal and external.
- Participates in audits as required/appropriate.
- Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities.
Qualifications Required For Pharmacovigilance Jobs:
- Bachelor’s Degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills, and abilities to perform the job.
- Safety Database systems and knowledge of medical terminology required.
- Good understanding of clinical trial process across Phases II-IV and/or post-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance.
- Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), Visio, email (Outlook), Team Share (or another management/shared content/workspace) and internet.
- Ability to work independently and in a team environment.
- Excellent communication and interpersonal skills, both written and spoken.
- Good organizational skills with proven ability to prioritize and work on multiple tasks and projects.
- Detail oriented with a high degree of accuracy and ability to meet deadlines.
