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Information And Documentation Officer -India

PLG groups
1-3 years
Not Disclosed
Remote, India, India
10 May 26, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Information and Documentation Officer – India

Location

India (Remote work possible)

Employment Type

Permanent Contract

Department

Life Cycle – Safety and Vigilance

Company

ProductLife Group


Role Overview

The Information and Documentation Officer is responsible for pharmacovigilance literature monitoring, scientific database screening, and documentation management within a global safety and vigilance hub.


Key Responsibilities

1. Literature Monitoring & Screening

  • Perform literature searches in international scientific databases

  • Conduct surveillance of local and international journals

  • Use databases such as PubMed and ADIS for identifying safety-related cases

  • Document and list relevant literature case findings


2. Documentation & Data Handling

  • Receive, store, and acknowledge documents from clients

  • Maintain structured documentation systems

  • Ensure proper archiving and traceability of safety-related documents


3. Quality Control & Compliance

  • Contribute to implementation of quality control systems

  • Track and follow up on quality performance of tasks

  • Participate in client audits and compliance checks


4. Collaboration & Reporting

  • Support pharmacovigilance hub operations

  • Coordinate with internal teams for literature monitoring outputs

  • Ensure timely reporting and structured data delivery


Required Qualifications

Education

  • Bachelor’s or Master’s degree in Pharmacy or Life Sciences


Experience

  • 1–3 years in Pharmacovigilance OR

  • Freshers with relevant pharmacovigilance knowledge


Technical Skills Required

  • Understanding of GVP Module VI (Good Pharmacovigilance Practices)

  • Knowledge of pharmacovigilance processes and literature writing

  • Familiarity with PubMed and ADIS databases

  • Strong pharmacology fundamentals

  • Advanced Microsoft Office skills:

    • Excel

    • Word

    • PowerPoint

    • Outlook

    • Teams

    • SharePoint


Soft Skills

  • Strong written and verbal communication in English

  • Attention to detail and accuracy

  • Ability to work in structured, compliance-driven environments

  • Analytical thinking and consistency

  • Ability to manage documentation workflows


Core Function

The role supports global drug safety monitoring by identifying and documenting adverse event information from scientific literature sources, ensuring compliance with pharmacovigilance regulations.