Looking for remote pharmacovigilance jobs in India? ProductLife Group (PLG) is hiring experienced Data Officers to join its Pharmacovigilance and Drug Safety team. This permanent remote opportunity is ideal for professionals with 2+ years of pharmacovigilance experience, particularly in ICSR data entry, case processing, regulatory submissions, and safety database management.
Candidates with a background in Pharmacy, Life Sciences, Industrial Biology, Chemistry, or related scientific disciplines who have experience working with global pharmacovigilance regulations can apply for this exciting opportunity.
Job Highlights
| Particular | Details |
|---|---|
| Company | ProductLife Group |
| Job Title | Data Officer |
| Job Type | Permanent |
| Location | India (Remote) |
| Department | Life Cycle โ Safety and Vigilance |
| Experience | Minimum 2 Years |
| Qualification | Bachelor’s Degree in Pharmacy, Life Sciences, Industrial Biology, Chemistry Engineering or related Science |
| Mode of Work | Remote |
| Application Mode | Online |
Key Responsibilities
As a Data Officer, you will be responsible for supporting global pharmacovigilance operations by performing:
- Data entry of Individual Case Safety Reports (ICSRs) into pharmacovigilance databases.
- Preparation of follow-up request emails and clarification requests.
- Submission of safety cases to competent health authorities.
- Performing database queries and preparing pharmacovigilance reports.
- Monitoring and downloading ICSRs from regulatory databases such as EudraVigilance and the MHRA Portal.
- Recording and updating medicinal product information in XEVMPD.
- Drafting and updating:
- Technical Agreements
- Safety Management Plans
- Client Templates
- SOPs
- Work Process Documents (WPDs)
- Training documents
- Supporting continuous process improvement initiatives.
- Maintaining compliance with global pharmacovigilance procedures.
Eligibility Criteria
Applicants should possess:
- Bachelor’s degree in:
- Pharmacy
- Life Sciences
- Industrial Biology
- Chemistry Engineering
- Related scientific discipline
- Minimum 2 years of pharmacovigilance experience.
- Previous experience with:
- ICSR data entry
- Quality Check (QC)
- Safety case processing
- Pharmacovigilance databases
- Experience working in service-provider/CRO environments is preferred.
Required Skills
Successful candidates should have:
- Strong knowledge of Pharmacovigilance principles.
- Understanding of:
- Good Pharmacovigilance Practices (GVP)
- Good Clinical Practice (GCP)
- FDA drug safety regulations
- EU Pharmacovigilance Regulations
- Knowledge of:
- Adverse Event Reporting
- Causality Assessment
- Medical Terminology
- Experience with pharmacovigilance databases.
- Strong documentation skills.
- Excellent English communication.
- Good organizational and teamwork abilities.
- Computer proficiency.
Why Join ProductLife Group?
Joining ProductLife Group offers professionals the opportunity to:
- Work remotely from anywhere in India.
- Build an international pharmacovigilance career.
- Gain exposure to European pharmacovigilance systems.
- Work with global pharmaceutical clients.
- Enhance regulatory and drug safety expertise.
- Be part of an experienced international safety team.
How to Apply
