PV Jobs at Syneos Health | Safety & PV Specialist | Life Sciences
Syneos Health, a premier global biopharmaceutical solutions organization, is currently hiring for the position of Safety & PV Specialist I (Literature Review) in Serilingampalli, Telangana. This PV job is a specialized role within the Pharmacovigilance and Safety family, focused on ensuring the continuous monitoring of drug safety through systematic literature screening and ICSR management. For professionals seeking a high-impact life science job, a Syneos Health career offers the opportunity to work at the forefront of clinical development, contributing to the safety of therapies that change lives globally.
- Position: Safety & PV Specialist I
- Location: Serilingampalli, Telangana, India.
- Function: Pharmacovigilance & Safety
About the Company
Syneos Health is the only fully integrated biopharmaceutical solutions organization designed to accelerate customer success. By combining Clinical Development and Commercial capabilities, Syneos Health provides unique insights that translate into better patient outcomes. A Syneos Health career means joining a “Total Self” culture that values diversity, peer recognition, and continuous professional progression.
Job Overview
The Safety & PV Specialist I is responsible for the critical task of literature screening to identify potential Individual Case Safety Reports (ICSRs). This PV job involves high-level data entry, medical coding using MedDRA, and ensures that all safety information is processed in compliance with global GVP (Good Pharmacovigilance Practices) and ICH GCP guidelines.
Key Responsibilities
- Literature Screening: Perform systematic reviews of scientific literature for safety signals and drug coding maintenance.
- ICSR Processing: Triage ICSRs, evaluate data for completeness, and enter information into the safety database with high accuracy.
- Medical Coding: Utilize MedDRA for coding events, medical history, and indications, ensuring compliance with global standards.
- Regulatory Compliance: Maintain the Pharmacovigilance System Master File and ensure all documents are submitted to the Trial Master File (TMF) as per SOPs.
- Signal Identification: Compile complete narrative summaries and identify information to be queried for expedited reporting.
Qualifications & Experience Required
This life science job requires a strong medical or scientific foundation combined with technical safety surveillance skills:
- Education: Bachelor’s Degree in Life Science.
- Specialized Experience: At least 2 years in Literature Review; candidates with additional experience in Clinical Trial Case Processing are preferred.
- Technical Knowledge: Proficiency in Safety Database systems and medical terminology is mandatory.
- Systems Proficiency: Experience with Drug Safety Triager Database and xEVMPD product records is highly desirable.
Securing a position as a Safety & PV Specialist I at Syneos Health is a strategic move for those specializing in PV jobs. This life science job offers a unique intersection of scientific analysis and regulatory surveillance, allowing you to influence safety outcomes for novel FDA and EMA-approved products. By pursuing a Syneos Health career, you gain access to world-class technical training and a supportive line management structure dedicated to your professional growth. If you have 2+ years of literature review experience and a passion for patient safety, apply today to join Syneos Health.
