- . Years of Experience: 4-6 years of relevant experience in Pharmacovigilance (PV),specifically in ICSR Quality Review and Regulatory Report Submissions
- Hands-on experience with the Argus Database is essential
To Approve schedule the reports in Argus database to the respective health authorities as applicable Submission of cases to Health Authorities, Business partners and Affiliates as applicable
Adherence to internal and external timelines for case processing to maintain regulatory reporting compliance To schedule and approval of regulatory reports based on reporting obligations.
Job Requirements:
- Years of Experience: 4-6 years of relevant experience in Pharmacovigilance (PV), specifically in ICSR Quality Review and Regulatory Report Submissions. Hands-on experience with the Argus Database is essential.
- Educational Qualification: B.Pharm, M.Pharm.
- Skills and Competencies:
- Solid knowledge of PV regulations and guidelines for health authority submissions.
- Expertise in quality assurance and compliance.
- Excellent attention to detail and analytical skills.
- Effective communication and time management abilities