- Contribute to completion of project milestones and organize own work to meet project task deadlines.
- Provide project teams with expertise on regulatory requirements and corporate policies governing documents for regulatory submission.
- Support Worldwide Strategy and Regulatory teams by providing analyses of post-marketing safety data, reviews of the medical literature, and similar related activities.
- Review case criteria to determine the appropriate workflow for case processing.
ONLY B. Pharm qualification.
Direct work experience in Pharmacovigilance, ICSR (Individual Case Safety Reports) processing of NO MORE THAN 2 years. B. Pharm freshers are also welcome to apply.
Decent knowledge of pharmacovigilance regulations, solid analytical skills, and very keen attention to detail!
Direct experience in the ARGUS safety database and with E2B case processing.
Good academic and/or extra-curricular accomplishments.
Apply through this Link