ProductLife Group is currently hiring Information & Documentation Officers (Literature Monitoring) for its remote Pharmacovigilance operations in India. This opportunity is ideal for B.Pharm, M.Pharm, and Life Science graduates who want to build a career in drug safety, pharmacovigilance literature monitoring, and medical information documentation.
The role focuses on literature surveillance, pharmacovigilance case identification, and database monitoring using PubMed and ADIS international literature databases. Candidates with 1โ3 years of pharmacovigilance experience or freshers with pharmacovigilance training are encouraged to apply.
This remote pharmacovigilance job in India offers exposure to global drug safety processes, GVP Module VI compliance, and international literature monitoring workflows, making it a strong entry point into pharmacovigilance and regulatory drug safety careers.
Author: Pharmabharat Editorial Team
Key Responsibilities
The selected Information & Documentation Officer (Literature Monitoring) will perform the following activities:
- Conduct literature searches in international databases such as PubMed and ADIS
- Perform literature monitoring and literature watch in local journals
- Identify and list pharmacovigilance cases reported in scientific literature
- Support pharmacovigilance signal detection and literature review processes
- Participate in client audits and pharmacovigilance compliance reviews
- Assist in implementing quality control systems for pharmacovigilance documentation
- Receive, store, and acknowledge documents sent by clients
- Maintain literature monitoring records and PV documentation
Eligibility Criteria
Educational Qualification
Candidates with the following qualifications can apply:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
- Life Sciences Graduate
This role is particularly suitable for candidates interested in pharmacovigilance literature monitoring jobs and drug safety careers.
Experience Required
- 1 to 3 years of experience in Pharmacovigilance
OR
- Freshers with pharmacovigilance training or knowledge
Candidates who have completed PV courses or training programs may also be considered.
Required Technical Skills
Applicants should have knowledge of:
- Good Pharmacovigilance Practices (GVP Module VI)
- Pharmacovigilance literature monitoring
- PubMed and ADIS literature databases
- Literature review and scientific publication analysis
Additional technical skills include:
- Microsoft Office Suite
- Excel
- Word
- PowerPoint
- Outlook
- Teams
- SharePoint
- Understanding of pharmacology and drug safety concepts
Preferred Skills
ProductLife Group is looking for candidates who demonstrate:
- Strong English communication skills
- Knowledge of pharmacovigilance workflows
- Ability to perform scientific literature analysis
- Attention to regulatory compliance and documentation quality
Job Location
Location: Remote (India)
This remote pharmacovigilance job allows professionals across India to work with global drug safety teams and international regulatory frameworks.
Salary (Estimated)
Based on market benchmarks for pharmacovigilance literature monitoring roles in India, the expected salary range is:
โน4,50,000 โ โน7,00,000 per year
Salary may vary depending on experience, pharmacovigilance training, and technical expertise.
Why Join ProductLife Group?
ProductLife Group is a global consulting organization supporting pharmaceutical, biotech, and medical device companies in regulatory, pharmacovigilance, and compliance services.
Benefits include:
- Exposure to global pharmacovigilance operations
- Opportunity to work on international literature monitoring projects
- Development of drug safety and regulatory expertise
- Remote working flexibility
- Career growth in PV, regulatory affairs, and medical information
How to Apply
