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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 – Hyderabad
Job Type: Full-Time
Job ID: 25104540
Updated: December 23, 2025

About Syneos Health

Syneos Health® is a leading integrated biopharmaceutical solutions organization dedicated to accelerating customer success. We transform clinical, medical affairs, and commercial insights into actionable outcomes for modern healthcare challenges.

With over 29,000 employees across 110 countries, Syneos Health provides an environment that fosters collaboration, innovation, and professional growth, enabling employees to contribute meaningfully to drug development and patient care worldwide.

Position Overview

The Safety & PV Specialist I (Literature Review) in Hyderabad is responsible for high-quality pharmacovigilance activities, focusing on literature review, case processing, and safety reporting. The role ensures accurate, timely, and regulatory-compliant management of Individual Case Safety Reports (ICSRs) while contributing to global safety standards and signal detection.

Key Responsibilities

Case Processing & Data Management:

  • Receive, triage, and enter ICSRs into PVG or designated safety databases.

  • Evaluate ICSRs for completeness, accuracy, and regulatory reportability.

  • Code adverse events, medical history, concomitant medications, and tests using MedDRA.

  • Identify and manage duplicate ICSRs and perform SAE reconciliations.

  • Maintain safety tracking for all assigned activities.

Literature Review & Regulatory Compliance:

  • Perform literature screening and reviews to support safety signal detection.

  • Validate and submit xEVMPD product records with accurate coding of indications.

  • Perform manual recoding of un-coded product and substance terms.

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

  • Participate in audits and inspections as required.

Collaboration & Documentation:

  • Compile narrative summaries and follow up on queries until resolved.

  • Ensure all documents are submitted to the Trial Master File (TMF) or Pharmacovigilance System Master File.

  • Coordinate with internal teams and external stakeholders for safety-related queries.

  • Maintain detailed documentation for regulatory readiness.

Quality & Process Improvement:

  • Apply quality control to literature case handling, database entries, and safety reports.

  • Contribute to process improvements in literature review and PV activities.

  • Implement safety reporting intelligence in routine activities.

Required Qualifications

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

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

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

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

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

  • Excellent organizational, communication, and interpersonal skills.

  • Ability to work independently and in a collaborative team environment.

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

Why Join Syneos Health

  • Contribute to global drug safety and pharmacovigilance initiatives.

  • Work in a collaborative, inclusive, and supportive environment.

  • Gain exposure to clinical trial safety operations and post-marketing pharmacovigilance.

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