BSc Life Sciences Jobs in Pharmacovigilance
Pharmacovigilance Specialist – Case Processing
Location: Hebbal, Bangalore, India
Company: ProPharma
Experience Required: 2 Years
Salary Range: ₹5 – ₹6 LPA
Employment Type: Full-Time
Interview Process: 2 Virtual Rounds + 1 Face-to-Face Interview
Are you passionate about patient safety and regulatory excellence in the pharmaceutical industry?
ProPharma, a global leader in life sciences consulting, is seeking a Pharmacovigilance Specialist – Case Processing to join our dynamic team in Bangalore. With over two decades of expertise, ProPharma partners with biotech, pharmaceutical, and medical device companies to bring innovative therapies to market — safely and effectively.
This is an exciting opportunity to contribute to impactful pharmacovigilance processes within India’s thriving biotech hub.
Key Responsibilities
As a Pharmacovigilance Specialist, you will be responsible for the complete and accurate processing of adverse event reports from clinical trials and post-marketed products. Your key duties will include:
• Case Processing: Review and manage Individual Case Safety Reports (ICSRs), assess seriousness, expectedness, and code events using MedDRA.
• Narrative Writing: Compose detailed, medically sound narratives for adverse event cases.
• Follow-Up: Identify, collect, and document follow-up information to ensure complete case data.
• Regulatory Compliance: Ensure cases are submitted within regulatory timelines per SOPs and global requirements.
• Client Communication: Provide timely updates to clients regarding case progress and status.
• Training & Documentation: Assist in the development and delivery of training materials related to pharmacovigilance.
• Quality Assurance: Peer-review cases for accuracy, quality, and consistency.
• Escalation: Report discrepancies or concerns to senior staff for prompt resolution.
• Continuous Learning: Stay informed on evolving pharmacovigilance regulations and global best practices.
Qualifications
• Education:
o Bachelor’s degree in Life Sciences (required)
o Advanced degree, RN, RPh, or PharmD (preferred)
• Experience:
o Minimum of 2 years in pharmacovigilance or related field
• Skills:
o Strong written, verbal, and interpersonal communication
o Exceptional attention to detail and accuracy
o Solid organizational and multitasking skills
o Basic understanding of MedDRA coding and pharmacovigilance principles
o Ability to work independently and collaboratively in a fast-paced environment
Why Join ProPharma?
• Impactful Work: Directly contribute to patient safety and global healthcare improvements
• Collaborative Environment: Join a supportive, cross-functional team in Bangalore’s biotech ecosystem
• Career Development: Gain access to ongoing training and growth opportunities
• Inclusive Culture: Thrive in a workplace that values diversity, equity, and authenticity
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