Responsible for the performance of the research study under the medical supervision of the Principal Investigator and the research director.
The research coordinator is responsible for the overall successful implementation and ongoing site management of the research studies.
Requirements
Candidates must have a minimum of two years prior clinical research experience, preferably with oncology clinical research; or a minimum of three years clinical experience (Medical Assistant, LPN, or RN in an oncology practice).
Candidates must have effective communication skills, be organized, detail oriented, and strong patient advocates.
Candidates must be available to travel to investigators meetings.
Valid Driver’s License in state of residency for travel to clinics.
Must comply with the Company Driver Safety Operations and Motor Vehicle Records Check Policy
Benefits
Medical and Prescription Drug Coverage
Vision & Dental Insurance
Employee Assistance Program (EAP)
Health Savings Account (HSA) & Flexible Spending Accounts