Job Description​

Responsibilities:

• Coordinate the conduct of research protocols in the hospital and clinic settings to ensure adherence to the protocol, institutional policies, and applicable federal and state regulations.  
• Screen and educate potential candidates about research protocols and obtains informed consent in accordance with institutional policy, IRB guidance, and applicable regulatory requirements.
• Participate in sponsor site visits and investigator meetings for assigned clinical trials which may involve occasional travel.
• Coordinate education for all involved personnel.
• Document patient interactions and completes study data entry.  Communicates to investigators on the results of procedures and tests.
• Record research activities in hospital tracking systems.
• Collect and prepares laboratory samples.
• Maintain investigational product accountability.
• Schedule participants follow up visits according to the study protocol.
• Schedule and supports sponsor-initiated monitor visits for periodic reviewing and querying of collected data in a timely fashion.
• Support study procedures in the Cardiac Cath lab. Multi campus coverage will be required.

Job Requirements

Applicable Experience:

Job Details

The best place to get care. The best place to give care. Saint Luke’s 12,000 employees strive toward that vision every day. Our employees are proud to work for the only faith-based, nonprofit, locally owned health system in Kansas City. Joining Saint Luke’s means joining a team of exceptional professionals who strive for excellence in patient care. Do the best work of your career within a highly diverse and inclusive workspace where all voices matter.

Join the Kansas City region's premiere provider of health services. Equal Opportunity Employer.