The Clinical Research Lead (CRL) is a field-based scientific leader responsible for driving the execution of Company clinical trials through exceptional investigator engagement and site performance management. This role involves combining deep scientific knowledge with strategic agility to influence investigators, elevate protocol understanding, and co-develop tailored enrollment strategies.

Conduct nutritional assessments and develop personalized dietetic plans, provide ongoing counseling and support, and maintain accurate client records while participating in virtual team meetings and training sessions.

The Senior Specialist Drug Safety Submission ensures the timely and accurate submission of global safety reports, such as ICSRs and PSURs, to regulatory authorities while supporting PV safety systems programming and maintenance. This role also involves reviewing global Safety management plans and other PV study documents to guarantee regulatory reporting accuracy.

The role involves performing site qualification, initiation, monitoring, management, and close-out visits to ensure compliance with regulatory standards, protocols, and GCP/GPP guidelines. Responsibilities also include evaluating site performance, managing data accuracy through source document review and query resolution, and ensuring proper handling of the Investigational Product.