ProPharma, a global leader in life sciences consulting and patient safety solutions, is hiring a Pharmacovigilance Specialist in India. This full-time position offers an opportunity to work on drug safety case processing, MedDRA coding, and global regulatory compliance, supporting some of the most advanced biotech and pharmaceutical programs worldwide.
With over 20 years of experience empowering the pharmaceutical, biotech, and medical device sectors, ProPharma provides an ideal environment for professionals passionate about pharmacovigilance and patient safety.
Key Responsibilities
As a Pharmacovigilance Specialist, you will be responsible for ensuring compliance with global safety regulations and maintaining the highest data integrity standards.
Your daily responsibilities will include:
- Managing individual case safety reports (ICSRs) for clinical trial and post-marketed products.
- Performing MedDRA coding, seriousness assessment, and expectedness evaluations.
- Composing detailed medical narratives and identifying missing or unclear information.
- Conducting case follow-ups and submitting expedited reports to regulatory authorities.
- Reviewing peer cases to maintain quality, consistency, and accuracy.
- Supporting the development of training materials and delivery sessions.
- Staying current with evolving global pharmacovigilance regulations.
Qualifications and Skills
Education
- Required: Bachelor’s degree in Life Sciences (Pharmacy, Biotech, or related field).
- Preferred: Advanced degree such as PharmD, RPh, or equivalent healthcare qualification.
Experience
- Minimum 2 years of experience in pharmacovigilance or related life sciences field.
Key Skills
- Strong written and verbal communication.
- Excellent attention to detail and analytical thinking.
- Knowledge of pharmacovigilance processes, regulatory compliance, and safety reporting.
- Ability to work independently and collaboratively within cross-functional teams.
Why Join ProPharma?
ProPharma values diversity, inclusion, and a collaborative environment where employees thrive professionally. The organization fosters continuous learning, innovation, and patient-centered impact.
Benefits include:
- Competitive salary and growth opportunities.
- Exposure to global PV systems and regulatory standards.
- A culture of learning, integrity, and teamwork.
- Work with a global network of drug safety professionals.
How to Apply
