Biomapas Hiring – PV Specialist (Case Processing) | Remote Jobs
Biomapas is hiring for the role of Pharmacovigilance Specialist – Case Processing for remote job opportunities. This position is suitable for candidates who have an interest or experience in drug safety and pharmacovigilance case processing. The role provides exposure to adverse event handling, safety documentation, and compliance‑driven workflows in a regulated environment.
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🏢 About Biomapas
Biomapas is a life sciences organization that provides regulatory, pharmacovigilance, and compliance support services to pharmaceutical and healthcare companies. The organization operates within structured quality systems and focuses on patient safety, data accuracy, and regulatory compliance. Professionals working at Biomapas gain experience in real‑world safety operations and global pharmacovigilance practices.
📊 Role Overview
- Position: PV Specialist (Case Processing)
- Department: Pharmacovigilance
- Location: Remote India
- Experience: 0 to 2 Years
- Qualification: B.Pharm
- Job Type: Full-Time
📋 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.
🎓 Qualification & Skill Required
- 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
⭐ Role Insight
- Pharmacovigilance case processing roles are critical in ensuring patient safety by accurately capturing and reporting adverse events. This position provides hands‑on exposure to real‑world safety data and regulatory‑driven processes. Working as a PV Specialist helps professionals understand how safety information contributes to risk assessment, regulatory decisions, and ongoing drug monitoring.
🎯 Ideal Candidates
- Candidates with pharmacovigilance experience
- Drug safety professionals seeking remote roles
- Life science graduates interested in PV case processing
- Professionals looking to work on global safety projects
📈 Growth Opportunities
With experience and continuous learning, professionals can progress into roles such as:
- Senior Pharmacovigilance Specialist
- Drug Safety Lead
- PV Quality Reviewer
- Pharmacovigilance Manager
💰 Expected Salary & Work Culture
- Salary Range: As per company standards
- Work Model: Fully Remote
- Compensation depends on experience level, role responsibilities, and internal company policies.
💡 Expert Tips
- Revise pharmacovigilance case processing concepts
- Understand ICSR workflows and documentation requirements
- Highlight safety experience clearly in your resume
- Be prepared to discuss case processing scenarios
🔗 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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📚 Career Guide
❓ Frequently Asked Questions – 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.
