ProPharma has announced an exciting Pharmacovigilance Specialist recruitment opportunity for professionals with experience in Individual Case Safety Report (ICSR) processing, adverse event case management, MedDRA coding, and regulatory safety reporting. This full-time opportunity is open to candidates across India, making it an excellent career option for Pharmacovigilance professionals looking to work with a globally recognized pharmaceutical consulting organization.
If you have experience in case processing, medical narrative writing, expedited reporting, and global pharmacovigilance regulations, this opportunity offers excellent career growth while working with global pharmaceutical, biotechnology, and medical device clients.
ProPharma Pharmacovigilance Specialist Recruitment 2026 โ Overview
| Particular | Details |
|---|---|
| Company | ProPharma |
| Job Title | Pharmacovigilance Specialist |
| Job Type | Full-Time |
| Location | India |
| Department | Pharmacovigilance |
| Experience | Minimum 2 Years |
| Qualification | Bachelor’s Degree in Life Sciences |
| Preferred Qualification | PharmD, RPh, RN, Advanced Degree |
| Working Model | Remote / Hybrid (Based on Location) |
| Job Posted | August 7, 2026 |
About ProPharma
For over 25 years, ProPharma has been helping pharmaceutical, biotechnology, and medical device companies accelerate product development while maintaining regulatory compliance. The company provides end-to-end consulting services across:
- Pharmacovigilance
- Regulatory Affairs
- Clinical Research
- Medical Information
- Quality & Compliance
- R&D Technology Solutions
ProPharma supports organizations throughout the complete product lifecycle using its Advise-Build-Operate model.
Key Responsibilities
As a Pharmacovigilance Specialist, you will be responsible for managing the complete lifecycle of Individual Case Safety Reports (ICSRs).
Your responsibilities include:
- Process adverse event cases from clinical trials and post-marketing sources
- Perform MedDRA coding for adverse events
- Assess seriousness and expectedness of safety events
- Conduct follow-up activities to obtain missing safety information
- Prepare and review high-quality medical narratives
- Generate client notifications related to safety cases
- Ensure expedited reporting compliance according to global regulations
- Review case quality for consistency and accuracy
- Support training activities and knowledge sharing
- Maintain compliance with SOPs and pharmacovigilance guidelines
- Escalate case discrepancies whenever necessary
- Stay updated with evolving global drug safety regulations
Required Qualifications
Candidates should possess:
- Bachelor’s Degree in Life Sciences (Mandatory)
Preferred qualifications include:
- PharmD
- Registered Pharmacist (RPh)
- Registered Nurse (RN)
- Advanced Degree in Life Sciences
Experience Required
Applicants should have:
- Minimum 2 years of Pharmacovigilance experience
- Hands-on experience in:
- ICSR Case Processing
- MedDRA Coding
- Seriousness Assessment
- Expectedness Assessment
- Narrative Writing
- Regulatory Reporting
- Pharmacovigilance SOP Compliance
Essential Skills
Successful candidates should demonstrate:
- Excellent written and verbal communication
- Strong analytical thinking
- High attention to detail
- Case quality review expertise
- Ability to prioritize multiple safety cases
- Team collaboration skills
- Knowledge of global pharmacovigilance regulations
- Problem-solving abilities
- Time management
Why Join ProPharma?
Working at ProPharma offers several advantages:
- Global Pharmacovigilance exposure
- Opportunity to work with leading pharmaceutical companies
- Remote and hybrid work flexibility
- Strong learning and development culture
- Inclusive workplace environment
- Career progression opportunities
- Exposure to international regulatory requirements
- Collaborative multidisciplinary teams
Who Should Apply?
This role is ideal for professionals currently working as:
- Pharmacovigilance Associate
- Drug Safety Associate
- Drug Safety Specialist
- PV Case Processor
- Safety Scientist
- ICSR Associate
- Medical Reviewer
- Pharmacovigilance Executive
Keywords for Job Seekers
- ProPharma Pharmacovigilance Specialist Jobs
- Pharmacovigilance Jobs India
- Drug Safety Jobs 2026
- ICSR Case Processing Jobs
- Remote Pharmacovigilance Jobs
- MedDRA Coding Jobs
- Pharmacovigilance Specialist Vacancy
- Life Sciences Pharmacovigilance Careers
- Drug Safety Associate Jobs India
- PV Specialist Recruitment
How to Apply

