Biomapas Pharmacovigilance Jobs 2026 | Remote PV Specialist (Case Processing) Hiring
Biomapas Pharmacovigilance Jobs - 2026 | Remote PV Specialist (Case Processing) Hiring
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(Biomapas Pharmacovigilance Jobs - 2026) |
Introduction
If you are looking to start or grow your career in pharmacovigilance and drug safety, this is an excellent opportunity. Biomapas (Delta PV division) is hiring Pharmacovigilance Specialists for remote roles.
With the increasing demand for drug safety professionals worldwide, this role offers strong exposure to ICSR case processing, regulatory compliance, and global pharmacovigilance operations. Whether you are a fresher or have some PV experience, this opportunity can help you build a solid career in clinical research and drug safety.
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About The Company
Biomapas is a globally recognized Contract Research Organization (CRO) specializing in pharmacovigilance, regulatory affairs, and clinical research services.
The company is headquartered in Europe and operates across multiple countries, supporting pharmaceutical, biotechnology, and medical device companies. Biomapas focuses on delivering high-quality drug safety and regulatory solutions aligned with global standards.
With a growing team of professionals worldwide, the company provides strong career growth, international exposure, and remote working opportunities for pharmacovigilance professionals.
Job Overview Summary
Biomapas is hiring for the role of Pharmacovigilance Specialist (Case Processing) under its Delta PV division. This is a remote job opportunity suitable for candidates with 0–2 years of experience.
The role involves working on ICSR lifecycle management, safety data processing, narrative writing, and regulatory reporting. Candidates will gain hands-on experience in pharmacovigilance workflows and global compliance standards.
This is a high-growth role for candidates aiming to build long-term careers in drug safety and regulatory domains.
Vacancy Details (Official)
- Position: Pharmacovigilance Specialist (Case Processing)
- Company: Biomapas (Delta PV Division)
- Job Type: Full-Time
- Location: Remote (Work From Home)
- Experience: 0–2 Years
- Industry: Pharmacovigilance / CRO
Responsibility Explanation
In this role, you will manage the complete lifecycle of Individual Case Safety Reports (ICSRs). This includes reviewing incoming safety reports, prioritizing cases, and entering data into safety databases.
You will write medically accurate clinical narratives, assess causality and seriousness of adverse events, and ensure compliance with global pharmacovigilance regulations.
Additionally, you will perform quality checks, handle follow-ups, and support reconciliation processes. This role requires attention to detail and a strong understanding of drug safety processes.
Eligibility Criteria (Official)
- Bachelor’s degree in Pharmacy / Life Sciences or related field
- 0–2 years of experience in pharmacovigilance or drug safety
- Freshers with strong PV knowledge can apply
Skills Required
Candidates should have a good understanding of pharmacovigilance concepts, especially the ICSR workflow. Basic knowledge of MedDRA coding and safety databases is preferred.
Strong communication skills, attention to detail, and analytical thinking are essential. Candidates should also be comfortable working remotely and managing tasks independently.
Proficiency in MS Office tools like Excel and Word is important for documentation and reporting.
Salary Estimate
The estimated salary for this role ranges between ₹3.5 LPA and ₹7 LP, depending on experience and skills.
Since this is a remote international CRO role, candidates may also receive performance bonuses and additional incentives based on productivity and quality metrics.
Interview Details (Official)
- Mode: Online / Virtual Interview
- Selection Process: Resume screening → Interview rounds → Final selection
Required Documents
Candidates should prepare the following documents:
- Updated Resume (CV)
- Educational Certificates
- Identity Proof (Aadhaar/PAN)
- Pharmacovigilance training certificates (if any)
- Internship or experience certificates
Make sure your resume highlights PV knowledge, ICSR experience, or relevant coursework.
How to Apply
Apply using the official link:
👉 https://apply.workable.com/biomapas/j/3098F45A73/
FAQs Section (Unique)
Q1. Is this a work-from-home pharmacovigilance job?
Yes, this is a 100% remote job.
Q2. Can freshers apply for this PV role?
Yes, freshers with strong pharmacovigilance knowledge can apply.
Q3. What is ICSR in pharmacovigilance?
ICSR stands for Individual Case Safety Report, used for reporting adverse drug reactions.
Q4. What is the experience required?
0–2 years of experience is required.
Q5. What is the salary range?
The estimated salary ranges between ₹3.5 LPA and ₹7 LPA.
Final Conclusion
Starting your pharmacovigilance career with Biomapas can be a smart move for long-term growth.
This remote opportunity provides hands-on experience in drug safety, ICSR processing, and global regulatory compliance. It is ideal for candidates who want to build careers in pharmacovigilance, clinical research, and regulatory affairs.
If you are serious about entering the drug safety domain, this is a high-value opportunity you should not miss.
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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