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Safety & Pv Trainee L Only For Delhi Ncr Freshers

0 years
Not Disclosed
10 Nov. 28, 2025
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 Trainee (Freshers – Delhi NCR Only)

Location: Gurugram, India
Job Type: Contractual (1-Year)
Updated: November 13, 2025

Employer: Syneos Health

Syneos Health is a leading global biopharmaceutical solutions organization dedicated to accelerating clinical, medical, and commercial outcomes for life-changing therapies. With operations in more than 110 countries and a workforce of 29,000 professionals, we are committed to enhancing patient outcomes and advancing modern healthcare innovation.

This position is designed exclusively for fresh graduates from Delhi NCR who are seeking to build a strong foundation in Pharmacovigilance (PV) and Drug Safety. The role offers structured training, hands-on exposure, and an opportunity to work with global safety operations teams.


Position Overview

As a Safety & Pharmacovigilance (PV) Trainee, you will support end-to-end case processing activities and contribute to maintaining high-quality safety reporting in compliance with global regulatory standards. This entry-level role is ideal for candidates passionate about drug safety, regulatory compliance, and clinical research operations.


Key Responsibilities

  • Enter safety information into PVG quality and tracking systems for case receipt and documentation.

  • Assist in processing Individual Case Safety Reports (ICSRs) as per SOPs and project-specific safety guidelines.

  • Perform ICSR triage, data validation, completeness checks, and regulatory reportability assessment.

  • Enter safety data into global safety databases accurately and efficiently.

  • Perform MedDRA coding for events, medical history, tests, and medications.

  • Prepare high-quality narrative summaries.

  • Identify data queries and ensure timely resolution.

  • Support expedited reporting activities in alignment with regulatory expectations.

  • Maintain safety tracking tools for assigned tasks.

  • Conduct literature screening and safety review when required.

  • Support coding and validation tasks for xEVMPD product records.

  • Manage recoding of product and substance terms as per safety standards.

  • Identify and manage duplicate ICSRs.

  • Contribute to SPOR and IDMP-related activities.

  • Participate in quality reviews and internal audits.

  • Ensure compliance with GCP, ICH, GVP guidelines, global safety regulations, and internal SOPs.

  • Upload essential documents to TMF and PV System Master File as required.

  • Collaborate with global teams, fostering a professional and constructive work environment.

  • Apply pharmacovigilance regulatory intelligence to daily tasks.


Required Qualifications

Education (Mandatory)

Candidates must have completed one of the following in 2025:

  • M.Pharm

  • Pharm.D

  • M.Sc + B.Pharm

  • BHMS

  • BDS

  • Ph.D. (Pharmacy)

Core Skills (Required)

  • Strong academic foundation in life sciences, healthcare, or pharmaceutical sciences.

  • Proficiency in Microsoft Office and Outlook.

  • Strong documentation, organizational, and multitasking skills.

  • Excellent written and verbal communication abilities.

  • High attention to detail, accuracy, and analytical mindset.

  • Ability to collaborate effectively in team-driven environments.

Preferred Skills (Added Advantage)

  • Familiarity with pharmacovigilance or drug safety concepts.

  • Knowledge of medical terminology or pharmacology.

  • Experience using safety databases or collaboration tools such as Visio or Team Share.


Experience Required

  • This role is specifically for freshers with qualifications completed in 2025.

  • No prior work experience is required, but internship or project exposure in Pharmacovigilance or Clinical Research is beneficial.


Employment Details

  • Contract Duration: 1 year (renewal subject to performance and business needs).

  • Work Culture: Inclusive, growth-driven, and aligned with Syneos Health’s Total Self culture.

  • Career Development: Structured training, mentoring, and opportunities for long-term progression.


Why Join Syneos Health

  • Work with a global leader in biopharmaceutical services.

  • Gain exposure to real-world pharmacovigilance operations.

  • Be part of a diverse workforce collaborating across therapeutic areas.

  • Opportunity to contribute to global clinical development and post-marketing safety programs.


Application

Apply through the official Syneos Health careers portal or explore more opportunities on ThePharmaDaily.com.

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