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Data Officer – Vaf 484

Product Life Group
Product Life Group
1-3 years
Not Disclosed
10 Dec. 31, 2025
Job Description
Job Type: Full Time Remote 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

Job Title: Data Officer – VAF 484
Location: India (Remote work possible)
Functional Area: Safety & Pharmacovigilance
Contract Type: Permanent
Experience Required: 1–3 years in Pharmacovigilance
Qualification: BPharm / MPharm

Company Overview:
Join a leading organization at the forefront of pharmacovigilance and patient safety. We provide integrated safety and vigilance services to global clients, supporting clinical trials, post-marketing surveillance, and regulatory compliance. Our teams ensure the highest standards of data management, safety reporting, and regulatory adherence, enabling life-saving therapies to reach patients efficiently and safely.

Role Summary:
The Data Officer is responsible for the efficient management of pharmacovigilance data, ensuring traceability, regulatory compliance, and accurate integration into client and internal safety tools. The role includes initial data handling, case entry, report generation, and supporting regulatory submissions, contributing to the effective operation of the safety and vigilance team.

Key Responsibilities:

Vigilance Data Management:

  • Manage generic and client-specific email inboxes related to vigilance cases.

  • Initial registration and triage of vigilance cases in internal tracking tools.

  • Identify duplicates and ensure accurate case entry, coding with MedDRA, and narrative writing.

  • Anonymize patient data as required and assess case seriousness with or without medically qualified support.

  • Prepare follow-up requests, clarifications, acknowledgements, and case closures.

  • Submit clinical and post-marketing cases to Competent Authorities, Ethics Committees, or client affiliates.

  • Notify clients according to Safety Data Exchange Agreements (SDEA) or Technical Agreements.

  • Generate summary reports and line listings from safety databases.

  • Analyze inclusion/exclusion criteria for cases from EV or MHRA ICSR downloads.

EudraVigilance & Regulatory Activities:

  • Set up ICSR and MLM filters under Case Specialist guidance.

  • Download, search, and submit ICSR data in EV and XEVMPD systems.

  • Conduct initial submissions to MHRA, FDA, and other Competent Authorities.

Writing & Documentation Support:

  • Draft and update technical agreements, safety management plans, and client templates.

  • Support the preparation and updating of SOPs and operating procedures relevant to pharmacovigilance activities.

Additional Responsibilities:

  • Extract data for KPI calculation and prepare activity monitoring reports.

  • Ensure effective communication with coordination teams to meet regulatory deadlines.

  • Provide weekly, monthly, quarterly, and annual reports to clients.

  • Participate in audits and present pharmacovigilance activities.

  • Ensure compliance with internal processes and proper implementation across the division.

Qualifications & Skills Required:

  • Bachelor’s or Master’s degree in Pharmacy (BPharm/MPharm).

  • 1–3 years of experience in pharmacovigilance or drug safety operations.

  • Knowledge of ICSR processing, MedDRA coding, EudraVigilance, and regulatory submissions.

  • Understanding of safety data management, clinical trial phases, and post-marketing surveillance.

  • Proficiency in Microsoft Office Suite and safety database tools.

  • Strong analytical, organizational, and communication skills.

  • Ability to manage multiple tasks and work in a fast-paced, matrixed environment.

Why Join:

  • Work with a global pharmacovigilance team and gain exposure to regulatory reporting across multiple markets.

  • Build expertise in safety database management, regulatory compliance, and pharmacovigilance workflows.

  • Opportunity to work remotely with international clients and diverse teams.