As Clinical Site Manager, you will be responsible for maximizing site performance and engagement in client-conducted clinical studies, leveraging clinical operational and therapeutic expertise to support their execution, while ensuring compliance with SOPs, GCP, and regulatory requirements. You will also develop strong relationships with investigators/staff to support clinical development programs.

As the primary sponsor liaison and advocate, you will plan, execute, manage and monitor regional clinical research projects, adapting and implementing project protocols, operational plans, and timelines. You will manage the day to day activities of a multidisciplinary project team, ensuring all decisions align with corporate, industry, sponsor and regulatory requirements.