Teams at Novotech

Manage site relationships and monitor clinical trial conduct to ensure participant safety and data integrity per ICH GCP, regulatory requirements, and sponsor/SOPs. Conduct site selection, initiation, monitoring and close-out (onsite or remote), support regulatory submissions, maintain TMF and clinical systems, drive recruitment, report visit findings, and assist project management for successful study execution.

The Inhouse Clinical Research Associate supports clinical team activities, manages study documentation, and ensures compliance with regulatory standards.

The Proposals Manager leads the proposal lifecycle, collaborates with teams to develop strategies, creates pricing models, and manages internal reviews for submissions.