Biomapas Hiring – PV Specialist (Case Processing) | Remote Jobs
Biomapas, through its Delta PV division, is hiring for the role of Pharmacovigilance Specialist – Case Processing. This remote opportunity is suitable for candidates with 1+ year of pharmacovigilance experience as well as fresh Life Sciences graduates who are looking to build a career in drug safety and pharmacovigilance operations.
The role focuses on end‑to‑end ICSR case processing, including case triage, data entry, narrative writing, causality assessment, and support for regulatory safety reporting. Candidates will gain hands‑on exposure to global pharmacovigilance workflows and compliance with international regulatory requirements.
This position offers a strong opportunity to develop practical expertise in safety data handling, regulatory compliance, and global PV processes, making it ideal for professionals seeking long‑term growth in the pharmacovigilance field.
Table of Contents
Job Overview
- Position: PV Specialist (Case Processing)
- Department: Pharmacovigilance
- Location: Remote India
- Experience: 0 to 2 Years
- Qualification: B.Pharm
- Job Type: Full-Time
Key Responsibilities – PV Specialist (Case Processing)
- Oversee and manage the end‑to‑end workflow of safety case reports to ensure timely and efficient processing.
- Perform initial triage of safety case reports to determine priority, completeness, and required follow‑up actions.
- Review, manage, and file source documents in accordance with applicable regulatory requirements and SOPs.
- Process safety cases including:
- Safety Database (SDB) data entry
- Case narrative writing
- Seriousness assessment
- Medical review, including causality and expectedness evaluation
- Assessment of regulatory reporting requirements
- Conduct follow‑up activities and manage internal and external queries related to safety case reports.
- Execute quality control (QC) checks on case data entry and processing to ensure accuracy, completeness, and compliance.
- Perform reconciliation of safety case reports to ensure consistency and completeness across data sources.
- Prepare line listings to summarize safety case data for reporting, tracking, and review purposes.
Required Skills & Qualifications
- Bachelor’s degree in Life Sciences or a related scientific discipline is required.
- Minimum 1 year of experience in pharmacovigilance or safety case processing within the pharmaceutical or CRO industry is preferred.
- Fresh graduates with a strong and relevant Life Sciences academic background may also be considered.
- Excellent written and verbal communication skills in English and the local language, with the ability to document safety information clearly, accurately, and compliantly.
- Strong proficiency in Microsoft Office applications, including Word, Excel, and Outlook, for safety documentation, tracking, and reporting activities
Why Join Biomapas?
- Strong opportunities for professional growth and long‑term career advancement within pharmacovigilance and drug safety.
- Work as part of a global, multicultural team, gaining exposure to international PV processes and standards.
- Eligibility for monthly performance bonuses, recognizing individual contribution and quality of work.
- Enjoy the flexibility of remote working, supporting work‑life balance while collaborating with global teams.
How to Apply
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer
This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.
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FAQ – PV Specialist (Case Processing)
1. Who can apply for this Pharmacovigilance Specialist role at Biomapas?
Candidates with a Bachelor’s degree in Life Sciences and at least 1 year of experience in pharmacovigilance or safety case processing can apply. Fresh life sciences graduates with strong academic backgrounds are also eligible.
2. Is this role suitable for fresh graduates?
Yes. While 1+ year of experience is preferred, motivated fresh graduates with relevant life sciences education and interest in pharmacovigilance are encouraged to apply.
3. What type of pharmacovigilance work will I handle?
You will support end‑to‑end ICSR case processing, including case triage, data entry, narrative writing, seriousness assessment, causality and expectedness evaluation, QC checks, follow‑ups, and reconciliations.
4. Is this a remote position?
Yes. This role offers remote work, allowing you to collaborate with an international PV team while maintaining work‑life balance.
5. Will I work with global safety databases and regulatory standards?
Yes. You will work in a global pharmacovigilance environment, following international safety regulations and SOPs, and supporting compliance‑driven safety reporting.
