Job Summary:
This position reports to the Sr. Director, Clinical Operations. Clinical Project Manager (CPM) will be responsible for protocol lead (PL) activities in multinational studies, working closely with the assigned CPM to oversee site-associated activities. This position will have CPM and PL responsibilities for small clinical studies (i.e. single center phase 1, or small phase 2 studies), with appropriate oversight by more senior clinical staff. International travel will be required. The position works closely with the Clinical Research Associate (CRA) and Clinical Assistant (CA) to ensure appropriate Clinical Trial Master File document archiving and tracking, and other study conduct activities. Expected assignments include PL activities for the NSCLC phase 2 and CPM/PL activities for a phase 1 RA study. Increasing responsibility and clinical project manager responsibilities is expected. Some travel, including internationally, will be required.
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