Work with a leading pharmaceutical company conducting clinical trials and ensuring regulatory compliance. This role involves monitoring trial sites, maintaining documentation, and supporting research teams in developing safe and effective medicines.

Skills 

Responsible for monitoring drug safety, analyzing adverse event reports, and ensuring compliance with global pharmacovigilance regulations to maintain patient safety and product quality.

Manage regulatory submissions and documentation for pharmaceutical products. Collaborate with global teams to ensure medicines meet international regulatory standards and approvals.

Act as a scientific expert connecting healthcare professionals with the company’s research and products. Provide medical insights, support clinical data discussions, and contribute to scientific communication.