Location: Gurugram / Hyderabad, India
Job Type: Full-Time | Office-Based
Company: Syneos Health
Job Requisition ID: 25104927
Experience Required: Minimum 8 Years
Freshers Eligible: No
About the Company
Syneos Health is a globally recognized, fully integrated biopharmaceutical and life sciences organization dedicated to accelerating customer success across clinical development and commercialization. The company partners with pharmaceutical, biotechnology, and healthcare innovators worldwide to support drug safety, regulatory compliance, and patient-centered healthcare advancement.
With operations across multiple countries and involvement in a majority of recently approved FDA and EMA therapies, Syneos Health continues to remain a leading employer in Pharmacovigilance, Drug Safety, Clinical Research, and Regulatory Operations.
Job Overview
Syneos Health is hiring experienced Pharmacovigilance professionals for the role of Principal Safety & PV Specialist – Literature Case Processing and Review. This is a senior-level drug safety position focused on global literature surveillance, literature case processing, safety data review, regulatory compliance, and pharmacovigilance operations management.
The role is ideal for candidates with strong expertise in literature monitoring, ICSR processing, safety databases, and pharmacovigilance compliance within clinical trials and post-marketing environments.
Key Responsibilities
Global Literature Surveillance & Review
Conduct systematic and ad-hoc literature searches using global biomedical databases including Embase, PubMed, and Medline
Identify and evaluate literature-based ICSRs and safety-related information
Develop, validate, and optimize literature search strategies for pharmacovigilance activities
Perform local literature review activities aligned with regional regulatory requirements
Extract, analyze, and summarize key medical and safety findings from scientific publications
ICSR Processing & Pharmacovigilance Operations
Triage and assess ICSRs for completeness, validity, accuracy, and regulatory reportability
Enter and manage safety data within pharmacovigilance databases
Code adverse events, concomitant medications, medical history, and laboratory data using standard medical terminologies
Prepare detailed narrative summaries for serious and non-serious adverse events
Conduct follow-up activities and resolve safety data queries
Support expedited reporting and compliance with global pharmacovigilance regulations
Safety Compliance & Regulatory Activities
Ensure compliance with ICH-GCP, GVP guidelines, SOPs, and global safety regulations
Support preparation of Safety Management Plans and program reports
Participate in audits, inspections, and internal review meetings
Coordinate reconciliation activities between clinical and safety databases
Ensure timely filing of relevant documentation in Trial Master File (TMF) and Pharmacovigilance System Master File (PSMF)
Leadership & Team Management
Allocate work and monitor deliverables across literature review and PV operations teams
Provide technical guidance and troubleshooting support to team members
Act as Subject Matter Expert (SME) for literature case processing and review activities
Support trend analysis and safety signal identification initiatives
Assist in training investigators and internal PV teams on safety reporting requirements
Educational Qualification
Candidates with the following educational backgrounds are eligible:
B.Pharm
M.Pharm
PharmD
BDS
BMS
Required Skills & Experience
Mandatory Requirements
Minimum 8 years of experience in Literature Case Processing and Pharmacovigilance
Prior Team Lead or supervisory experience in Drug Safety operations
Strong expertise in literature databases including Embase and PubMed
Hands-on experience with ICSR processing and safety review workflows
Knowledge of clinical trial safety requirements across Phase II–IV studies and post-marketing surveillance
Technical Skills
Safety database management systems knowledge
Understanding of medical terminology and coding standards
Familiarity with ICH-GCP, GVP, and global PV regulations
Proficiency in Microsoft Office Suite, Outlook, Visio, and collaborative workspace tools
Soft Skills
Strong analytical and decision-making abilities
Excellent communication and presentation skills
Ability to manage multiple projects and deadlines effectively
Strong organizational and leadership capabilities
Work Location
Gurugram, Haryana, India
Hyderabad, Telangana, India
This is an office-based role with minimal travel requirements.
Why Join Syneos Health?
Opportunity to work with one of the world’s leading global CROs and life sciences organizations
Exposure to global pharmacovigilance operations and multinational safety projects
Career growth opportunities in Drug Safety, Medical Review, and PV Leadership
Collaborative work environment focused on innovation, compliance, and scientific excellence
Important Note for Applicants
This is a senior-level Pharmacovigilance opportunity and is not suitable for freshers or entry-level candidates. Candidates applying for this role should possess extensive hands-on experience in literature surveillance, literature case processing, and global drug safety operations.
About ThePharmaDaily
For more verified Pharmacovigilance jobs, Drug Safety openings, Clinical Research careers, Regulatory Affairs vacancies, and Pharma industry opportunities across India and globally, visit ThePharmaDaily.com regularly.
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