Are you looking to build a rewarding career in pharmacovigilance (PV)? 🚀
Here’s an exciting opportunity for aspiring and experienced professionals to work as a Pharmacovigilance Specialist (Case Processing) in a fully remote setup.
This role is ideal for candidates from life sciences backgrounds who want to contribute to global drug safety and patient well-being.
🏢 About the Organization
Delta PV, a reputed pharmacovigilance service provider based in Istanbul, Türkiye, is now part of the Biomapas group (since August 2025).
With a strong global footprint, the organization delivers high-quality drug safety and risk management solutions to pharmaceutical and biotech clients worldwide 🌍.
📍 This opportunity is open to candidates based in:
- India
- Algeria
- Tunisia
💼 Job Role: Pharmacovigilance Specialist (Case Processing)
This is a full-time remote position focused on Individual Case Safety Report (ICSR) processing.
As a PV Specialist, you will play a critical role in ensuring that adverse event data is accurately processed, evaluated, and reported according to global regulatory standards.
🔑 Key Responsibilities
📊 Case Processing & Management
- Process and manage ICSRs efficiently
- Perform accurate data entry into safety databases
- Write clear, concise, and medically relevant narratives
⚠️ Safety Evaluation
- Conduct seriousness assessments
- Perform causality and expectedness evaluations
- Support medical review processes
🔍 Quality & Compliance
- Ensure compliance with global regulatory guidelines (ICH, GVP)
- Perform quality checks (QC) on safety cases
- Reconcile safety data for accuracy and completeness
📁 Documentation & Reporting
- Maintain proper source documentation
- Prepare line listings and reports
- Handle follow-ups and query resolution
🤝 Collaboration
- Work closely with PV team leads and managers
- Identify risks related to timelines and quality
- Support process improvements and SOP updates
🎓 Eligibility Criteria
✔️ Bachelor’s degree in Life Sciences (B.Pharm, M.Pharm, Pharm.D, Biotechnology, etc.)
✔️ Minimum 1 year PV experience OR freshers with relevant training
✔️ Strong understanding of ICSR processing
✔️ Good communication skills in English
✔️ Proficiency in MS Office
🌟 Why This Job is a Great Opportunity
🌐 Work from Anywhere
Enjoy the flexibility of a fully remote role, improving work-life balance.
📈 Career Growth
Gain hands-on exposure to global pharmacovigilance operations.
🤝 International Exposure
Collaborate with professionals across multiple countries.
💰 Additional Benefits
- Monthly performance bonuses 💸
- Continuous learning & upskilling 📚
- Supportive and collaborative work culture
🧠 Skills You’ll Develop
- ICSR case processing expertise
- Medical narrative writing
- Regulatory compliance (ICH & GVP)
- Data reconciliation & quality control
- Safety database handling
🚀 Career Path After This Role
This role opens doors to advanced positions such as:
- Senior PV Specialist
- Drug Safety Associate
- Signal Detection Specialist
- Risk Management Specialist
- Regulatory Affairs Associate
💡 Tips to Get Selected
- Highlight ICSR processing experience clearly in your resume
- Mention tools like Argus, ARISg, Veeva Safety
- Demonstrate strong attention to detail
- Prepare for workflow-based interview questions
📢 Final Thoughts
The demand for pharmacovigilance professionals is growing rapidly due to increasing regulatory requirements and global drug safety awareness 💊
This remote opportunity is ideal for:
- Freshers with PV training
- Experienced professionals looking for global exposure
If you’re aiming for a stable, impactful, and future-proof career, pharmacovigilance is one of the best paths to choose in 2026.
🔗 Apply Now
👉 https://apply.workable.com/biomapas/j/3098F45A73/
