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Safety & Pv Trainee L Only For Delhi Ncr Freshers

1+ years
Not Disclosed
10 Nov. 27, 2025
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 & Pharmacovigilance (PV) Trainee – Freshers, Delhi NCR

Location: Gurugram, Delhi NCR
Job Type: Contract (1 Year, with continuation based on performance)
Updated: November 13, 2025
Job ID: 25102900

Company Overview

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization, dedicated to accelerating clinical development and optimizing patient outcomes. With a global workforce of 29,000 employees across 110 countries, Syneos Health delivers innovative solutions across clinical, medical affairs, and commercial functions, placing patients and customers at the center of every project.

Why Join Syneos Health

  • Structured career development and training for fresh graduates

  • Exposure to global pharmacovigilance (PV) processes and regulatory compliance

  • Inclusive “Total Self” culture encouraging authenticity and collaboration

  • Opportunity to work on FDA-approved, EMA-authorized, and other global clinical programs

Role Overview

The Safety & PV Trainee will gain hands-on experience in pharmacovigilance and safety operations for clinical trials and post-marketing programs. This role is ideal for fresh graduates from healthcare and life sciences backgrounds looking to launch their career in drug safety.

Key Responsibilities

  • Enter and track Individual Case Safety Reports (ICSRs) in PVG quality and tracking systems

  • Assist in processing ICSRs according to SOPs and safety plans

  • Triage ICSRs, evaluate completeness, accuracy, and regulatory reportability

  • Enter data into safety databases; code events, medications, medical history, and tests

  • Compile narratives and identify missing information for queries

  • Support timely reporting of expedited cases in compliance with regulations

  • Conduct literature review, MedDRA coding, and xEVMPD record validation

  • Identify and manage duplicate ICSRs and SPOR/IDMP-related activities

  • Maintain Trial Master File (TMF) and Pharmacovigilance System Master File documentation

  • Participate in audits, ensuring compliance with SOPs, GCP, ICH, and GVP guidelines

  • Collaborate with internal and external project teams to support PV operations

Qualification Requirements

Education & Eligibility:

  • M.Pharm, Pharm.D, M.Sc + B.Pharm., BHMS, BDS, or Ph.D. (Pharmacy) – 2025 graduates only

Core Skills:

  • Strong healthcare or scientific background

  • Proficiency in Microsoft Office Suite and Outlook

  • Excellent organizational, documentation, and multitasking skills

  • Strong written and verbal communication

  • High attention to detail and accuracy

  • Team collaboration skills

Preferred Qualifications:

  • Familiarity with pharmacovigilance databases, medical terminology, and drug safety processes

  • Exposure to collaboration tools (Visio, Team Share, etc.)

About Syneos Health’s Impact

  • Supported 94% of novel FDA-approved drugs and 95% of EMA-authorized products

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

Learn more: syneoshealth.com

How to Apply

Fresh graduates from Delhi NCR meeting the above criteria are encouraged to apply. Join Syneos Health’s Talent Network to stay updated on additional pharmacovigilance and clinical operations opportunities.