Safety & Pharmacovigilance Specialist I – Literature Review
Location: Pune, India
Job ID: 25104540
Industry: Pharmacovigilance | Drug Safety | Clinical Research
Employment Type: Full-time
Experience Required: Minimum 2+ Years
Updated On: December 23, 2025
Syneos Health®, a global leader in integrated biopharmaceutical solutions, is hiring a Safety & Pharmacovigilance (PV) Specialist I – Literature Review to support global drug safety and pharmacovigilance operations. This role is well suited for professionals with hands-on experience in literature screening, safety case processing, and regulatory compliance across clinical trial and post-marketing environments.
The position plays a key role in ensuring accurate safety data collection, evaluation, and reporting in compliance with global regulatory requirements.
Pharmacovigilance & Case Processing
Receive, track, and process Individual Case Safety Reports (ICSRs) in accordance with SOPs and project-specific safety plans.
Perform triage and evaluation of ICSRs for completeness, accuracy, and regulatory reportability.
Enter, code, and update safety data in the safety database, including adverse events, medical history, concomitant medications, and laboratory tests.
Prepare clear and compliant narrative summaries and manage follow-up queries to resolution.
Literature Review & Safety Surveillance
Conduct end-to-end literature screening and review for safety-relevant information.
Perform literature case processing and identify valid ICSRs from scientific publications.
Support drug coding, maintenance of drug dictionaries, and MedDRA coding activities.
Regulatory & Data Management
Validate and submit xEVMPD product records, including accurate MedDRA coding of indication terms.
Perform manual recoding of products and substances derived from ICSRs.
Identify, assess, and manage duplicate ICSRs.
Support SPOR/IDMP-related pharmacovigilance activities.
Quality, Compliance & Audits
Conduct quality review of ICSRs to ensure regulatory compliance and data integrity.
Ensure timely submission of safety documentation to the Trial Master File (TMF) and Pharmacovigilance System Master File (PSMF).
Maintain compliance with global safety regulations, ICH-GCP, GVP, SOPs, and Work Instructions.
Participate in internal, sponsor, and regulatory audits as required.
Collaboration & Communication
Work closely with internal and external stakeholders to support safety deliverables.
Apply regulatory intelligence and safety reporting updates across all assigned activities.
Education
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related healthcare discipline.
Equivalent combination of education and relevant pharmacovigilance experience will be considered.
Experience
Minimum 2+ years of experience in pharmacovigilance literature review.
Candidates with combined experience in literature case processing and clinical trial case processing are strongly preferred.
Technical Skills
Experience with Drug Safety Triage databases for literature review activities.
Working knowledge of safety databases and medical terminology.
Understanding of clinical trial phases II–IV and post-marketing safety requirements.
Familiarity with global safety regulations, including ICH-GCP and GVP guidelines.
Professional Competencies
Proficiency in MS Word, Excel, PowerPoint, Outlook, and shared content management tools.
Strong attention to detail with high accuracy and compliance focus.
Excellent written and verbal communication skills.
Ability to manage multiple tasks, meet deadlines, and work independently or within a team.
Contribute to safety programs supporting over 94% of novel FDA-approved drugs and 95% of EMA-authorized products.
Gain exposure to global pharmacovigilance operations across clinical and post-marketing programs.
Benefit from structured training, career progression, and a supportive professional environment.
Be part of a diverse, inclusive, and people-focused global organization.
Syneos Health is a fully integrated biopharmaceutical solutions organization with more than 29,000 professionals across 110+ countries. The company partners with biopharmaceutical innovators to accelerate the development and commercialization of life-changing therapies.
Job responsibilities may evolve based on project and business requirements.
Equivalent qualifications and transferable skills will be considered.
Syneos Health is an equal opportunity employer committed to diversity, equity, inclusion, and accessibility.
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