ProPharma Hiring 2026 – PV Specialist & Regulatory Medical Writer Jobs
Looking for pharmacovigilance or medical writing jobs in India?
ProPharma is hiring experienced professionals for Pharmacovigilance Specialist (Case Processing) and Principal Regulatory Medical Writer roles.
These positions offer an excellent opportunity to work with a global life sciences consulting organization supporting pharmaceutical, biotech, and medical device companies.
About ProPharma
ProPharma has over 25 years of experience supporting drug development and regulatory success through its advise–build–operate model. The company provides services across pharmacovigilance, regulatory sciences, clinical research, and quality compliance.
With a strong focus on innovation, flexibility, and inclusion, ProPharma offers a modern work environment with remote and hybrid options.
Job Overview
- Company: ProPharma
- Location: India
- Employment Type: Full-time
- Work Mode: Remote / Hybrid
- Open Positions:
- Pharmacovigilance Specialist (JR 10312)
- Principal Regulatory Medical Writer (JR 10313)
Open Positions Details
🔹 Pharmacovigilance Specialist – Case Processing (JR 10312)
- Experience: Minimum 2 years
- Qualification: Bachelor’s in Life Sciences (Advanced degree preferred)
Key Responsibilities:
- Process adverse event cases (clinical & post-marketing)
- Perform MedDRA coding & case assessment
- Write medical narratives
- Ensure compliance with global safety regulations
- Submit expedited reports to regulatory authorities
Principal Regulatory Medical Writer (JR 10313)
- Experience: Minimum 7 years
- Qualification: Degree in medical/scientific discipline
Key Responsibilities:
- Author clinical and regulatory documents (CSR, IND, NDA, BLA, etc.)
- Lead cross-functional coordination
- Mentor junior writers
- Ensure compliance with ICH and regulatory guidelines
- Manage timelines and client expectations
Skills Required
For Pharmacovigilance Specialist:
- Knowledge of drug safety & case processing
- Strong communication & analytical skills
- Attention to detail and problem-solving ability
For Medical Writer:
- Expertise in clinical documentation & regulatory writing
- Strong understanding of ICH, FDA, and global guidelines
- Advanced MS Word and document structuring skills
- Leadership and project management abilities
Benefits & Perks
- 🌍 Work with global pharma and biotech clients
- 🏠 Flexible remote / hybrid work model
- 📈 Strong career growth and mentoring support
- 🤝 Inclusive and diverse work culture
- ⚖️ Healthy work-life balance
How to Apply
Apply directly through the official ProPharma career links:
Pharmacovigilance Specialist (JR 10312)
Principal Regulatory Medical Writer (JR 10313)
📌 All applications are reviewed manually by the recruitment team.
Why You Should Join ProPharma
ProPharma offers a chance to work on high-impact global healthcare projects, contributing directly to drug safety and regulatory success.
Whether you’re processing safety cases or writing complex regulatory submissions, you will play a key role in bringing new therapies to market while building a rewarding career.
FAQs
1. What experience is required for PV Specialist?
Minimum 2 years in pharmacovigilance or case processing.
2. What is required for Medical Writer role?
At least 7 years of regulatory/clinical writing experience.
3. Is remote work available?
Yes, ProPharma offers remote and hybrid work options.
4. Are freshers eligible?
No, both roles require prior experience.
5. How are applications reviewed?
Applications are reviewed by real recruiters (no AI screening).
