To support clinical development in oncology, the full-time salaried Oncology Research Services Director will manage scientific operations, focusing on protocol development, clinical study plans, and regulatory submissions while working remotely.Key responsibilitiesDevelop protocols for clinical studies and prepare clinical development plansDraft clinical scientific documents for regulatory submissions and monitor ongoing study dataLead clinical matrix teams and represent exploratory development on project teamsRequired qualificationsDegree in a scientific/life sciences field; Pharm.D.
or Ph.D.
preferredMinimum of 8 years of experience in oncology research or related fieldDemonstrated experience leading clinical development programs in oncologyExperience with global regulatory interactions and submissionsStrong understanding of oncology clinical endpoints and trial design