Syneos Health Career – Safety & PV Specialist I Hyderabad
Ready to elevate your Syneos Health career and make a meaningful impact in global pharmacovigilance? Explore one of the most rewarding medical jobs in Hyderabad with Syneos Health – a world leader in biopharmaceutical solutions. As a Safety & PV Specialist I, you’ll be part of a dynamic team at Syneos Health Hyderabad, contributing to drug safety, patient well-being, and innovative healthcare outcomes.
Job Details:
- Job Title: Safety & PV Specialist I
- Location: Hyderabad, India (Hybrid)
About the Company:
Syneos Health® is a global leader in integrated biopharmaceutical solutions, dedicated to transforming medical innovation into real-world impact. With over 29,000 professionals across 110 countries, Syneos Health accelerates customer success through clinical development, medical affairs, and commercial strategies. The company’s Total Self culture empowers individuals to thrive authentically, supporting growth and collaboration across all levels. Whether you’re pursuing your first Syneos Health career or advancing within, this is where passion meets purpose.
Qualifications to upskill your Syneos Health Career:
- Bachelor’s or Master’s degree in Dental Science or Medicine(BDS / BMS / MBBS)
- 2.5 to 4 years of relevant pharmacovigilance experience.
- Proficiency in safety databases such as Argus or Aris-G.
- Strong knowledge of ICH, GVP, and regulatory standards.
- Excellent communication skills and attention to detail.
Job Description:
As part of your Syneos Health career, the Safety & PV Specialist I role offers the opportunity to shape the future of drug safety. Based in Syneos Health Hyderabad, you’ll handle ICSR case processing, regulatory reporting, and data validation within a collaborative, innovation-driven environment. This position combines scientific rigor with a global impact, making it one of the most exciting medical jobs in Hyderabad today.
Key Responsibilities to upskill your Syneos Health Career:
- Perform ICSR case processing, including booking, triage, and data entry.
- Enter case information into PVG quality and tracking systems for ICSR receipt and monitoring.
- Evaluate data accuracy, completeness, and regulatory reportability.
- Code medical history, adverse events, and laboratory tests using Argus or Aris-G databases.
- Prepare detailed narrative summaries and resolve safety queries.
- Generate accurate and timely expedited safety reports per global standards.
- Conduct literature screening, MedDRA coding, and dictionary maintenance.
- Validate and submit xEVMPD product records; handle duplicate ICSR management.
- Support SPOR/IDMP-related activities and ensure TMF documentation compliance.
- Adhere to global drug safety regulations, SOPs, and ICH/GVP guidelines.
- Collaborate professionally with internal and external teams, contributing to audits and inspections.
