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HomeJobsBDSExciting Pharmacovigilance Job at Syneos Health | BDS Candidates Apply Now!

Exciting Pharmacovigilance Job at Syneos Health | BDS Candidates Apply Now!

Pharmacovigilance Job at Syneos Health

What makes a career in pharmacovigilance so rewarding? Syneos Health offers an exciting opportunity for professionals eager to make a difference in the life sciences sector. The Safety & PV Specialist I position in Gurugram is perfect for those passionate about drug development and commercialisation. This Pharmacovigilance Job allows individuals to contribute significantly to public health by ensuring the safety and efficacy of pharmaceutical products.

About Syneos Health:

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. The company partners with innovators at every point across the drug development and commercialisation continuum, helping them navigate complexity, anticipate change, and accelerate progress. With a commitment to developing its people and fostering an inclusive culture, Syneos Health aims to shape solutions that dramatically impact lives.

Job Details:

  • Job Title: Safety & PV Specialist I – Literature Case Processing
  • Location: Gurugram, India
  • Job Requisition ID: 25111538
  • Time Type: Full-time

Job Description:

The Safety & PV Specialist I will be responsible for entering information into PVG quality and tracking systems, assisting in the processing of Individual Case Safety Reports (ICSRs), and ensuring compliance with regulatory requirements. The role requires a strong understanding of safety database systems and the clinical trial process.

Key Responsibilities:

  • Enter information into PVG quality and tracking systems for receipt and tracking ICSR as required.
  • Assist in the processing of ICSRs according to Standard Operating Procedures (SOPs).
  • Perform literature screening and review for safety, drug coding, and maintenance of drug dictionary in the Pharmacovigilance Job.
  • Validation and submission of xEVMPD product records.
  • Identification and management of duplicate ICSRs at Syneos Health.
  • Ensure all relevant documents are submitted to the Trial Master File (TMF).
  • Foster constructive and professional working relationships with all project team members.
  • Participate in audits as required.

Eligibility Criteria for the Pharmacovigilance Job:

  • 2+ years of experience in Literature Data entry along with MLM experience.
  • BDS / Pharm D Degree or Equivalent.
  • Knowledge of safety database systems and medical terminology.
  • Good understanding of clinical trial processes across Phases II-IV.
  • Proficiency in Microsoft Office Suite and internet tools.
  • Excellent communication and interpersonal skills.
  • Detail-oriented with a high degree of accuracy.

This position at Syneos Health offers a significant opportunity for qualified candidates to contribute to impactful drug development initiatives. Interested individuals are encouraged to apply at the earliest before the deadline.

CLICK HERE TO APPLY NOW

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