Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Safety & Pv Specialist I (Literature Review)

Syneos Health
Syneos Health
2+ years
preferred by company
10 Feb. 5, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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 & Pharmacovigilance Specialist I – Literature Review

Updated: February 3, 2026
Location: Gurgaon, Haryana, India
Job ID: 25104540
Employment Type: Full-Time
Department: Pharmacovigilance / Drug Safety / Medical Safety


About Syneos Health®

Syneos Health® is a global, fully integrated biopharmaceutical solutions organization committed to accelerating customer success. By combining clinical development, medical affairs, and commercial expertise, Syneos Health delivers innovative solutions that address evolving healthcare and regulatory landscapes worldwide.

With a patient-centric Clinical Development model and operations across more than 110 countries, Syneos Health focuses on simplifying processes, fostering collaboration, and advancing therapies that improve patient outcomes.

Work Here Matters Everywhere.


Job Overview

The Safety & Pharmacovigilance Specialist I – Literature Review supports global pharmacovigilance operations with a primary focus on safety literature screening, adverse event identification, and Individual Case Safety Report (ICSR) processing. This role ensures accurate safety data capture, regulatory compliance, and high-quality safety reporting across clinical trial and post-marketing environments.


Key Responsibilities

  • Enter and track safety information in pharmacovigilance quality and tracking systems for ICSRs

  • Assist in ICSR processing in accordance with SOPs, work instructions, and project-specific safety plans

  • Triage ICSRs and assess case data for completeness, accuracy, and regulatory reportability

  • Enter and maintain safety data in validated safety databases

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

  • Compile clear and complete case narratives and follow up on data queries until resolution

  • Support timely and accurate expedited safety reporting in compliance with global regulatory requirements

  • Maintain safety tracking logs for assigned activities

  • Perform systematic literature screening and review to identify safety information

  • Support drug coding activities, drug dictionary maintenance, and MedDRA coding

  • Validate and submit xEVMPD product records with appropriate MedDRA-coded indications

  • Perform manual recoding of unclassified product and substance terms arising from ICSRs

  • Identify and manage duplicate safety cases

  • Support SPOR / IDMP-related pharmacovigilance activities

  • Conduct quality review of ICSRs to ensure compliance and data integrity

  • Ensure timely filing of all safety documentation in the Trial Master File (TMF) and Pharmacovigilance System Master File (PSMF)

  • Maintain compliance with global safety regulations including ICH-GCP, GVP, and applicable drug, biologic, and device regulations

  • Collaborate effectively with internal and external stakeholders across global project teams

  • Participate in audits and inspections as required

  • Apply current regulatory intelligence to all safety reporting activities


Required Qualifications & Experience

  • Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related discipline

  • Minimum 2+ years of experience in pharmacovigilance literature review

  • Experience in literature case processing and clinical trial case processing is strongly preferred

  • Hands-on experience with Drug Safety Triage or similar literature review databases

  • Working knowledge of safety databases and medical terminology

  • Solid understanding of clinical trial phases (II–IV) and post-marketing safety requirements

  • Knowledge of global pharmacovigilance regulations, including ICH-GCP, GVP, and safety reporting standards

  • Proficiency in Microsoft Office applications (Word, Excel, PowerPoint) and collaboration tools

  • Strong written and verbal communication skills

  • Excellent organizational and time-management abilities

  • High attention to detail with the ability to manage multiple priorities and meet regulatory timelines

  • Ability to work independently and collaboratively within cross-functional teams


Why Join Syneos Health

  • Structured career growth within global pharmacovigilance operations

  • Exposure to complex clinical trial and post-marketing safety programs

  • Comprehensive training and development opportunities

  • Inclusive Total Self culture promoting diversity, equity, and belonging

Over the past five years, Syneos Health has supported:

  • 94% of all novel FDA-approved drugs

  • 95% of EMA-authorized products

  • Over 200 studies across 73,000 sites and more than 675,000 clinical trial participants


Additional Information

This job description is not exhaustive and responsibilities may evolve based on business needs. Syneos Health is an equal opportunity employer committed to compliance with global employment legislation and accessibility standards, including reasonable accommodations where applicable.


Job Family Summary – Pharmacovigilance & Safety

Roles within the Pharmacovigilance & Safety function provide expertise across medical safety activities, including adverse event review, literature surveillance, signal detection, and risk management. These roles support clinical development and post-marketing programs while ensuring global regulatory compliance and patient safety.