Freshers Lifesciences jobs at Syneos – Apply Now for the Safety & PV Specialist Role
Syneos Health is hiring a Safety & PV Specialist I for literature case review in Gurugram, India. This full-time role is ideal for life science graduates with experience in pharmacovigilance and a strong understanding of biomedical databases. Contribute to global safety reporting by identifying and summarizing safety-relevant literature while working in a collaborative, purpose-driven environment.
Job Title: Safety & PV Specialist I (Review of Literature Cases)
Location: IND–Gurugram
Job ID: 25003447
About the Company:
Syneos Health® is a leading, fully integrated biopharmaceutical solutions organization built to accelerate customer success. Operating across more than 110 countries with over 29,000 employees, Syneos Health combines clinical development, real-world evidence, and commercialization services into a unified offering. The company partners with emerging biotech and global pharmaceutical leaders to deliver tailored solutions, reduce complexity, and bring innovative therapies to market faster. At Syneos Health, collaboration, innovation, and patient-focused outcomes drive every decision, making it a trusted partner in advancing healthcare worldwide.
Job Description:
Syneos Health is seeking a Safety & PV Specialist I to support pharmacovigilance through literature review. This position focuses on identifying and summarizing safety-relevant data from biomedical literature sources such as PubMed and Embase, in compliance with global regulatory requirements. The role also involves processing Individual Case Safety Reports (ICSRs), maintaining databases, and supporting regulatory submissions for clinical trials and post-marketing programs.
Key Responsibilities for Freshers Lifesciences jobs at Syneos
- Conduct systematic and ad-hoc literature searches in biomedical databases
- Extract and summarize key safety information from identified literature
- Validate literature search strategies for pharmacovigilance purposes
- Conduct local literature searches and reviews
- Understand global and local regulatory requirements for literature review
- Enter data into PVG systems and track ICSRs
- Assist in ICSR processing, triage, and data quality review
- Code medical history, events, tests, and medications using standard dictionaries (e.g., MedDRA)
- Generate narrative summaries and resolve data queries
- Perform xEVMPD submissions and manual recoding of product terms
- Maintain safety tracking activities and identify duplicates
- Conduct activities related to SPOR/IDMP and quality review of ICSRs
- Ensure TMF compliance for clinical and post-marketing documentation
- Maintain adherence to SOPs, GVP, GCP, ICH guidelines, and regulatory standards
- Collaborate with internal and external stakeholders and participate in audits
- Apply regulatory intelligence to safety reporting activities
Qualifications for Freshers Lifesciences jobs at Syneos
- Bachelor’s degree in life sciences, pharmacy, nursing, or related field
- Experience with safety databases and medical terminology
- Understanding of clinical trials (Phases II–IV) and post-marketing safety practices
- Familiarity with ICH GCP, GVP, and safety reporting regulations
- Proficiency in Microsoft Office, Outlook, Visio, and shared workspaces
- Strong written and verbal communication skills
- Excellent organizational and multitasking abilities
- Detail-oriented with high accuracy and ability to meet deadlines
- Ability to work independently and within a team environment
Keywords: Safety & PV Specialist, Pharmacovigilance, Drug Safety, Literature Review, Regulatory Compliance, Clinical Trials
