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Safety & Pv Coordinator (Hyderabad Office-Based)

Syneos Health
Syneos Health
1 years
Not Disclosed
Hyderabad, India
10 Feb. 18, 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 (PV) Coordinator – Hyderabad (Office-Based)

Location: Hyderabad, India (Office-Based)
Experience Required: Minimum 1 Year in Pharmacovigilance (PMS & Spontaneous Cases)
Education: B.Pharm or M.Pharm (Mandatory)
Industry: Pharmacovigilance | Drug Safety | Clinical Research
Job ID: 25105305

Job Overview

A leading global biopharmaceutical solutions organization is hiring a Safety & Pharmacovigilance (PV) Coordinator for its Hyderabad office. This role is ideal for professionals with hands-on experience in post-marketing surveillance (PMS), spontaneous case processing, and Individual Case Safety Reports (ICSRs).

The selected candidate will support global pharmacovigilance operations, ensure regulatory compliance, and contribute to high-quality safety data management aligned with ICH, GVP, and global regulatory standards.

Key Responsibilities

  • Enter and manage safety data within pharmacovigilance quality and tracking systems.

  • Process Individual Case Safety Reports (ICSRs) according to SOPs and project-specific safety plans.

  • Perform ICSR triage and evaluate case data for completeness, accuracy, and regulatory reportability.

  • Conduct data entry into safety databases (LSMV preferred; Argus acceptable).

  • Perform MedDRA coding for adverse events, medical history, indications, and concomitant medications.

  • Prepare and compile complete narrative summaries for ICSRs.

  • Identify missing information, generate queries, and ensure timely follow-up.

  • Support expedited reporting in compliance with global regulatory requirements.

  • Perform literature screening and safety review activities.

  • Maintain drug dictionaries and manage product coding activities.

  • Validate and submit xEVMPD product records, including MedDRA indication coding.

  • Identify and manage duplicate ICSRs.

  • Support SPOR and IDMP-related activities.

  • Conduct quality review of safety cases.

  • Ensure submission of safety documentation to Trial Master File (TMF) and Pharmacovigilance System Master File (PSMF) as applicable.

  • Participate in audits and maintain inspection readiness.

  • Apply regulatory intelligence to ensure compliant safety reporting practices.

Required Experience and Qualifications

  • Minimum 1 year of experience in Pharmacovigilance, specifically PMS and spontaneous case processing.

  • Practical experience handling ICSRs and safety database systems (LSMV preferred; Argus acceptable).

  • Strong knowledge of MedDRA coding and medical terminology.

  • Understanding of:

    • ICH GCP guidelines

    • GVP regulations

    • Clinical trial safety requirements (Phase II–IV)

    • Post-marketing pharmacovigilance regulations

  • Education: B.Pharm or M.Pharm (mandatory requirement).

  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), Outlook, and shared work platforms.

  • Strong organizational skills with the ability to manage multiple tasks and deadlines.

  • Detail-oriented with high accuracy standards.

  • Ability to work independently and collaboratively in cross-functional teams.

  • Excellent written and verbal communication skills.

Organization Overview

The organization operates across 110+ countries with more than 29,000 professionals globally. Over the past five years, it has supported 94% of Novel FDA Approved Drugs and 95% of EMA Authorized Products, contributing to more than 200 clinical studies across 73,000 sites and over 675,000 clinical trial patients worldwide.

The company follows a patient-centric development model and promotes diversity, regulatory excellence, and continuous professional growth.

Job Summary

The Safety & PV Coordinator plays a critical role in pharmacovigilance operations by ensuring accurate processing, coding, quality review, and regulatory reporting of safety data. The role requires compliance with global drug safety regulations, attention to detail, and effective coordination across clinical and regulatory teams.

aWhy Apply via ThePharmaDaily.com

ThePharmaDaily.com connects qualified pharmacovigilance and drug safety professionals with verified global opportunities in clinical research, regulatory affairs, medical writing, and pharmaceutical development.

Apply now to advance your career in pharmacovigilance and drug safety operations.