Job Description
- 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.
Qualifications
Qualifications
Must-Have
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!
Nice-to-Have
Direct experience in the ARGUS safety database and with E2B case processing.
Good academic and/or extra-curricular accomplishments.
Apply through this Link