Provide clinical support, leadership, and supervision to the Multiple Myeloma Disease-Oriented Team (DOT)
Oversee patient-related clinical activities of the research office
Supervise a team of Clinical Research Coordinators, Research Nurses, and/or Data Coordinators
Handle multiple projects simultaneously and work independently using initiative and good judgment
Assist with review of current research trials and development of operational protocols
Collect, prepare, process, analyze, and submit participant data and samples
Recruit, screen, and enroll trial participants, collect complex information, perform medical assessments
Monitor program budgets and approve unit expenditures
Schedule logistics and secure resources for clinical research trials
Exercise supervisory authority over at least 2.0 FTE employees
Serve as a subject matter expert and main point of contact for clinical research participants

Minimum 2 years of experience coordinating clinical trials in hematologic malignancies
SOCRA Certification in Clinical Research Required
Clinical Research Certification required to be obtained within 6 months of hire. CCRP, ACRP, CCRA, CCRC, ACRP-CP are all comparable certifications that are acceptable as well.
4 years of experience coordinating clinical trials in hematologic malignancies preferred
Experience coordinating and/or managing Multiple Myeloma clinical trials preferred
Experience using EPIC Electronic Health Record software preferred
Supervisory/Management experience preferred
Bachelor's Degree preferred, focus: Biomedical or social science, or related field

Clinical Team Manager

Key skills