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Safety & Pv Specialist L (Qc Experience)

Syneos Health
Syneos Health
3+ years
preferred by company
10 Jan. 12, 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 (QC Experience)

Location: Gurugram, Haryana, India
Employment Type: Full-Time
Job Category: Pharmacovigilance / Drug Safety
Experience Required: 3+ Years
Job ID: 25104167
Last Updated: January 8, 2026

About the Company

Syneos Health® is a globally recognized, fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. With expertise spanning clinical development, medical affairs, and commercial solutions, Syneos Health supports pharmaceutical and biotech companies in delivering innovative therapies that improve patient outcomes worldwide. Operating across 110+ countries with a workforce of over 29,000 professionals, Syneos Health is committed to excellence, agility, and diversity.

Job Overview

The Safety & Pharmacovigilance Specialist I (QC Experience) will play a critical role in pharmacovigilance operations, ensuring high-quality case processing, regulatory compliance, and accurate safety reporting. This role involves handling clinical trial, post-marketing, and spontaneous case safety data while maintaining compliance with global safety regulations and internal quality standards.

Key Responsibilities

  • Perform end-to-end Individual Case Safety Report (ICSR) processing in compliance with SOPs, GVP, ICH, and regulatory requirements

  • Conduct quality control (QC) review of ICSRs for completeness, accuracy, and regulatory reportability

  • Enter, code, and maintain safety data in pharmacovigilance databases, including MedDRA and drug dictionaries

  • Compile detailed and compliant case narratives and follow up on safety queries until resolution

  • Support expedited and non-expedited safety reporting within defined timelines

  • Identify, assess, and manage duplicate safety cases

  • Perform literature screening and safety data review

  • Support xEVMPD submissions, SPOR/IDMP-related activities, and product data maintenance

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

  • Participate in internal and external audits and inspections as required

  • Collaborate cross-functionally with internal and external stakeholders to support safety operations

Required Qualifications

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

  • Minimum 3 years of hands-on experience in Pharmacovigilance case processing with Quality Control exposure

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

  • Strong knowledge of pharmacovigilance regulations including ICH-GCP, GVP, MedDRA, and global safety guidelines

  • Proficiency in safety databases and medical terminology

  • Advanced working knowledge of Microsoft Office tools (Word, Excel, PowerPoint, Outlook)

  • Excellent written and verbal communication skills

  • Strong attention to detail with the ability to manage multiple priorities under tight timelines

Preferred Skills

  • Experience with regulatory submissions and safety reporting systems

  • Prior exposure to audits and inspection readiness activities

  • Ability to work independently as well as in a collaborative, global team environment

Why Join Syneos Health

  • Work on the majority of novel FDA- and EMA-approved products globally

  • Access structured career development, technical training, and progression opportunities

  • Inclusive and diverse workplace culture that supports authenticity and growth

  • Opportunity to contribute to therapies that positively impact global patient health

Equal Opportunity Statement

Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, age, sexual orientation, disability, veteran status, or any other legally protected status. Employment decisions are based solely on business needs, merit, and qualifications.