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Safety & Pv Specialist I (Literature Review)

Syneos Health
Syneos Health
2+ years
Not Disclosed
10 Jan. 7, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Safety & PV Specialist I – Literature Review

Location: India – Gurugram
Job Type: Full-Time
Job ID: 25104540
Updated: December 23, 2025

About Syneos Health

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization committed to accelerating customer success. By transforming clinical, medical affairs, and commercial insights into actionable outcomes, we address modern healthcare challenges while keeping patients at the center of our work.

With 29,000 employees across 110 countries, Syneos Health fosters a collaborative and inclusive culture, enabling employees to innovate, grow professionally, and impact global drug development.

Position Overview

The Safety & PV Specialist I (Literature Review) in Gurugram is responsible for literature-based pharmacovigilance activities, ICSR processing, and safety reporting. This role ensures accurate, timely, and compliant management of safety data, supports signal detection, and maintains adherence to regulatory standards across clinical and post-marketing programs.

Key Responsibilities

ICSR Management & Data Entry:

  • Receive, triage, and process ICSRs according to SOPs and project-specific safety plans.

  • Evaluate case data for completeness, accuracy, and regulatory reportability.

  • Enter adverse events, medical history, concomitant medications, and lab tests into safety databases.

  • Identify and manage duplicate ICSRs, perform quality reviews, and compile narrative summaries.

Literature Review & Regulatory Compliance:

  • Conduct literature screening and reviews for safety signals.

  • Validate and submit xEVMPD product records, ensuring accurate MedDRA coding of indications.

  • Recode un-coded product and substance terms from ICSRs.

  • Maintain compliance with SOPs, GCP, ICH, and GVP guidelines.

Collaboration & Documentation:

  • Ensure timely submission of all relevant documents to the Trial Master File (TMF) or Pharmacovigilance System Master File.

  • Work with internal teams and external stakeholders for data clarification and follow-up.

  • Participate in audits and inspections as required.

Quality & Process Improvement:

  • Apply safety reporting intelligence to all activities.

  • Maintain awareness of project budgets and timelines.

  • Contribute to continuous improvement in literature review and PV processes.

Required Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or equivalent.

  • Minimum 2+ years of literature review experience; experience in literature case processing and clinical trial case processing preferred.

  • Familiarity with pharmacovigilance databases, medical terminology, and safety regulations.

  • Knowledge of clinical trial phases II–IV and post-marketing safety requirements.

  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and collaboration tools.

  • Strong organizational, communication, and interpersonal skills.

  • Ability to work independently and in a team environment.

  • Detail-oriented with high accuracy and adherence to deadlines.

Why Join Syneos Health

  • Engage in global pharmacovigilance operations and literature review activities.

  • Collaborate with experienced professionals in a supportive and inclusive culture.

  • Opportunities for mentorship, career growth, and professional development.

  • Contribute to patient safety and drug development on an international scale.