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.
