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Data Officers (Pharmacovigilance)

2+ years
₹6 – ₹9 LPA
10 Aug. 5, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Data Officers (Pharmacovigilance)
Location: India or Philippines (Remote, working Eastern USA Time Zone)
Department: Safety and Vigilance – Life Cycle
Employment Type: Permanent

Job Summary:
ProductLife Group is hiring Data Officers (Pharmacovigilance) to support global pharmacovigilance operations. This fully remote role requires availability during Eastern USA Time Zone hours. As a Data Officer, you will be responsible for the intake, processing, tracking, and quality control of Individual Case Safety Reports (ICSRs), supporting both local and global PV activities while ensuring regulatory compliance across US and EU markets.

Key Responsibilities:

  • Perform intake, triage, processing, and data entry of ICSRs in line with client and regulatory timelines

  • Manage client-specific email boxes for case handling and follow-up

  • Coordinate case processing tasks including assignment and reconciliation activities

  • Respond to queries from clients and safety reporters regarding pharmacovigilance cases

  • Support local safety activities and contribute to local PV compliance as needed

  • Assist during audits and inspections, including implementation of action plans

  • Ensure all pharmacovigilance data is compliant with GVP, GCP, FDA, and EMA requirements

Required Qualifications:

  • Bachelor’s or Master’s degree in Medicine, Pharmacy, Nursing, or Life Sciences

  • Minimum 2 years of pharmacovigilance experience (case processing and QC)

  • Previous experience working with tight deadlines and high-volume case environments

  • Strong knowledge of US and EU PV regulations, GVP, and FDA reporting requirements

  • Proficient in adverse event reporting and causality assessment

Key Skills:

  • Excellent verbal and written communication skills

  • Strong organizational skills and attention to detail

  • Ability to work independently and within remote teams

  • Effective time management and prioritization

  • Adaptable, process-oriented, and able to work under pressure

  • Experience with safety databases (e.g., Argus, ArisG, Veeva Vault Safety, etc.)

Estimated Salary:
₹6 – ₹9 LPA (India) / ₱600,000 – ₱900,000 annually (Philippines) – based on experience and location

Join ProductLife Group and contribute to the evolving field of global pharmacovigilance, while working remotely with a team dedicated to safety and compliance.