Key Responsibilities:

• Processing and quality reviewing of Individual Case Safety Reports (ICSR).
• Ensuring compliance with regulatory guidelines and company SOPs.
• Assisting in the preparation of safety reports and other pharmacovigilance documentation.
• Collaborating with cross-functional teams to address pharmacovigilance-related queries.
• Contributing to the continuous improvement of pharmacovigilance processes.

Qualifications:

• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related field.
• 1 to 5 years of experience in pharmacovigilance case processing and quality reviewing.
• Strong understanding of pharmacovigilance regulations and guidelines.
• Excellent attention to detail and quality focus.
• Good communication and organizational skills.
• Ability to work effectively in a team environment.

Application Process: Interested candidates can share their CV with Manjunatha at manjunatha.sp@arcolab.com.