Global healthcare consulting company ProPharma has announced openings for the position of Pharmacovigilance Coordinator in India. This is an excellent opportunity for pharmacy, life sciences, and healthcare graduates seeking a career in pharmacovigilance, drug safety, and adverse event case processing.
The position offers exposure to global pharmacovigilance operations, including safety database management, literature screening, duplicate checks, and client communication activities. Candidates with prior industry exposure are preferred, although motivated freshers with relevant knowledge may also find this role attractive.
Job Details
- Position: Pharmacovigilance Coordinator
- Company: ProPharma
- Job Type: Full-Time
- Work Model: Remote/Hybrid (depending on proximity to office locations)
- Locations: India, Croatia, Serbia
- Industry: Pharmacovigilance, Drug Safety, Regulatory Affairs
- Experience: Preferred 1 year of industry experience
- Education: Post-secondary education in pharmacy, life sciences, or related disciplines
About ProPharma
ProPharma is a global provider of consulting and outsourcing solutions across the pharmaceutical, biotechnology, and medical device industries. For over 25 years, the company has supported organizations throughout the product lifecycle with services in:
- Regulatory Sciences
- Clinical Research Solutions
- Pharmacovigilance
- Medical Information
- Quality & Compliance
- R&D Technology Services
The company partners with organizations using an advise-build-operate model to accelerate drug and medical device development programs.
Pharmacovigilance Coordinator Responsibilities
The selected candidates will be responsible for:
- Managing assigned pharmacovigilance mailboxes and client communications
- Performing duplicate searches and initial case book-in activities
- Screening and redacting source documents containing protected health information (PHI)
- Supporting literature surveillance activities
- Conducting initial triage of regulatory authority database searches
- Sending draft safety reports to clients for review
- Entering essential safety information into pharmacovigilance databases
- Processing adverse event reports and maintaining case documentation
- Supporting internal case processing activities and additional pharmacovigilance tasks
Required Skills
Candidates should possess:
- Strong verbal and written communication skills
- Excellent interpersonal skills
- Good computer and keyboarding proficiency
- Strong organizational and prioritization abilities
- High attention to detail
- Ability to work independently and in collaborative environments
Educational Qualifications
Candidates with the following backgrounds are encouraged to apply:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Other healthcare or life sciences qualifications
Experience Requirements
- Preferred: Minimum one year of pharmacovigilance or pharmaceutical industry experience
- Knowledge of drug safety case processing and adverse event reporting is advantageous
Why Join ProPharma?
Working at ProPharma offers several benefits:
- Opportunity to work with global pharmaceutical and biotechnology clients
- Exposure to international pharmacovigilance operations
- Flexible remote and hybrid work opportunities
- Inclusive and diverse work environment
- Career growth in drug safety and regulatory sciences
- Experience across end-to-end safety case processing activities
Estimated Salary
Based on current market standards for pharmacovigilance coordinator roles in India, the estimated compensation may range between:
₹4.5 LPA – ₹7.5 LPA
Actual compensation may vary depending on experience, skills, and location.
How to Apply
