Are you detail-oriented, passionate about pharmacovigilance, and eager to make a difference in patient safety? ClinChoice India is expanding its Case Processing team in Bangalore, offering professionals with 2–10 years of experience the opportunity to contribute to high-quality safety data management and grow their careers in drug safety.

This role provides the chance to work with a global team while applying your expertise in ICSR case processing, MedDRA coding, narrative writing, and quality review.

Key Responsibilities

• Process and review Individual Case Safety Reports (ICSRs) in compliance with global regulatory requirements.
• Perform MedDRA coding and narrative writing for adverse event cases.
• Conduct quality reviews of case processing deliverables.
• Ensure timely entry, tracking, and reporting of safety data in relevant databases.
• Collaborate with global safety and pharmacovigilance teams.

Required Qualifications

• Experience: 2–10 years in pharmacovigilance case processing.
• Strong knowledge of ICSR processing, MedDRA coding, narrative writing, and safety database systems.
• Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Medicine, or related fields.
• Attention to detail, strong analytical skills, and ability to work in a global team.

Benefits of Joining ClinChoice

• Opportunity to contribute to global patient safety initiatives.
• Career growth in a rapidly expanding pharmacovigilance team.
• Exposure to global safety standards and regulatory compliance processes.
• Collaborative and supportive work environment.

Application Process

Interested candidates can apply by sharing their updated CV to:
📧 madhurima.das@clinchoice.com or megha.chinnappa@clinchoice.com