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Safety & Pv Specialist L (Qc Experience)

Syneos Health
Syneos Health
3 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 – Quality Control (QC)

Updated: February 3, 2026
Location: Gurgaon, Haryana, India
Job ID: 25104167
Employment Type: Full-Time
Industry: Pharmacovigilance / Drug Safety / Clinical Research

About Syneos Health®

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

With a patient-centric Clinical Development model, Syneos Health continuously streamlines processes to enhance efficiency, quality, and collaboration. With over 29,000 professionals across 110 countries, the organization is committed to advancing therapies that improve and save lives.

Work Here Matters Everywhere.


Job Overview

The Safety & Pharmacovigilance Specialist I (QC Experience) is responsible for end-to-end pharmacovigilance case processing and quality control activities across clinical trial, post-marketing surveillance (PMS), and spontaneous reporting environments. This role ensures accurate, timely, and compliant safety data management in accordance with global regulatory standards.


Key Responsibilities

  • Enter, track, and manage Individual Case Safety Reports (ICSRs) in pharmacovigilance quality and safety databases

  • Perform case processing activities in compliance with SOPs, work instructions, and project-specific safety plans

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

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

  • Compile high-quality narrative summaries and identify missing or inconsistent data for follow-up queries

  • Ensure timely resolution of case queries and accurate expedited safety reporting

  • Maintain safety tracking logs for assigned pharmacovigilance activities

  • Conduct literature screening and review for safety data identification

  • Support drug dictionary maintenance and medical coding activities

  • Validate and submit xEVMPD product records with accurate MedDRA coding

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

  • Identify, assess, and manage duplicate safety cases

  • Support SPOR / IDMP-related pharmacovigilance activities

  • Perform quality control (QC) review of ICSRs

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

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

  • Participate in internal and external audits and inspections as required

  • Collaborate effectively with cross-functional internal and external stakeholders


Required Qualifications & Experience

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

  • Minimum 3 years of hands-on experience in pharmacovigilance case processing with Quality Control (QC) exposure

  • Proven experience handling Clinical Trial, Post-Marketing Surveillance (PMS), and Spontaneous cases

  • Strong working knowledge of safety databases and medical terminology

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

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

  • Proficiency in Microsoft Office applications (Word, Excel, PowerPoint), Outlook, and collaborative document management systems

  • Ability to work independently as well as collaboratively within cross-functional teams

  • Excellent written and verbal communication skills

  • Strong organizational, prioritization, and time-management abilities

  • High attention to detail with the ability to meet strict regulatory timelines


Why Join Syneos Health

  • Structured career development and progression opportunities

  • Comprehensive technical and therapeutic area training

  • Supportive leadership and peer recognition programs

  • Inclusive Total Self culture promoting authenticity and belonging

  • Exposure to global clinical trials and post-marketing safety programs

Over the past five years, Syneos Health has supported:

  • 94% of all novel FDA-approved drugs

  • 95% of EMA-authorized products

  • 200+ studies across 73,000 sites and over 675,000 trial participants


Additional Information

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


Job Family Summary – Pharmacovigilance & Safety

Roles within the Pharmacovigilance & Safety function provide expert safety oversight across clinical development and post-marketing programs. Professionals contribute to safety signal detection, risk management, aggregate reviews, and regulatory compliance while supporting clinical development teams and pharmacovigilance operations.