Join a team dedicated to advancing oncology clinical trials. In this role, you’ll manage global studies, oversee vendors, collaborate with multi-disciplinary teams, and ensure compliance with regulatory standards. Make an impact in cancer research!

Accelerate progress at clinical trials by managing phases 1-3 in oncology. Collaborate with global teams, overseeing vendors, budgets, and protocols from concept to completion, ensuring compliance with regulatory standards.

Drive the development of innovative small molecule drug products through collaboration with cross-functional teams and external partners, ensuring alignment with regulatory standards while leading strategic initiatives in a fast-paced biotech environment.