Join Syneos Health as a Safety & PV Specialist II (Literature Review) | Explore Pharmacovigilance Jobs
Looking to grow your career in Pharmacovigilance Jobs with a global biopharma leader? Syneos Health Careers offers a rewarding opportunity for professionals passionate about safety science and literature review. The position of Safety & PV Specialist II (Literature Review) is ideal for candidates eager to advance in PV Jobs in India, contributing to global safety reporting, compliance, and clinical excellence. Join Syneos Health and be part of a company that’s shaping the future of patient safety worldwide.
Job Details:
- Job Title: Safety & PV Specialist II (Literature Review)
- Location: Global / PV Jobs in India (Remote or Hybrid options may apply)
About the Company :
Syneos Health® is a leading global biopharmaceutical solutions organization dedicated to accelerating innovation and patient safety. With a team of 29,000 professionals across 110 countries, Syneos Health has built a strong reputation for advancing healthcare outcomes through integrated clinical, medical affairs, and commercial solutions. The company’s Total Self culture empowers every employee to bring their authentic self to work, promoting diversity, inclusion, and continuous growth. Whether you’re pursuing Pharmacovigilance Jobs or other opportunities through Syneos Health Careers, you’ll join a team that’s redefining how therapies reach patients faster, making it a unique place for pharmacovigilance opportunities.
Job Description For Pharmacovigilance Jobs
The Safety & PV Specialist II (Literature Review) plays a key role in ensuring global patient safety through comprehensive literature surveillance. This position is designed for professionals seeking Pharmacovigilance Jobs within a dynamic and collaborative global team. You will identify, evaluate, and manage safety-related data, ensuring full regulatory compliance and quality across all pharmacovigilance processes as you explore roles in pharmacovigilance.
Key Responsibilities – PV Jobs in India
- Conduct systematic and ad-hoc literature searches in databases such as Embase, PubMed, and Medline for ICSR identification and safety-relevant data.
- Extract and summarize critical safety information from literature sources when tackling pharmacovigilance tasks.
- Develop and validate search strategies for pharmacovigilance purposes.
- Conduct local literature reviews aligned with global regulatory requirements.
- Enter safety data into PVG systems for ICSR processing and tracking.
- Process ICSRs according to SOPs and safety management plans.
- Compile narrative summaries, assess data quality, and ensure accurate reporting in pharmacovigilance jobs.
- Collaborate with data management teams for database reconciliation.
- Participate in audits and maintain compliance with ICH GCP, GVP, and SOP standards.
Qualifications – Pharmacovigilance Jobs Requirements
- Bachelor’s or Postgraduate Degree in Life Sciences, Pharmacy, Nursing, or equivalent.
- 3+ years of pharmacovigilance experience, with a focus on literature case reviewing (global + local).
- Strong understanding of GVP Module VI and global safety databases in pursuing pharmacovigilance career options.
- Excellent communication and interpersonal skills.
- Proficiency in Microsoft Office Suite, Visio, and collaborative tools.
- Strong organizational and multitasking abilities.
- Minimal travel required (up to 5%).
