Oncology Clinical Research Coordinator — Patient-Centric Trials

Saint Luke's; Kansas City (MO); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Medical health plans

Tuition reimbursement

PTO & Welfare plans

Retirement contributions

Employee assistance program

Job summary

Saint Luke’s Hospital in Kansas City, MO is seeking a Clinical Research Coordinator to join our research team to assist with providing and coordinating care for patients active in various research studies.

You will prepare the site for conduct of the study, identify potential study participants, conduct informed consent, assist with scheduling labs and appointments, gather and record study related data, and provide patient education for various research studies.

Qualifications

• Bachelor's degree required.
• Experience coordinating clinical trials preferred.

Responsibilities

• Supports, facilitates and coordinates the daily clinical trial activities.
• Works under the direction of the clinical Principal Investigator (PI).
• Collaborates with PI, department, sponsor and institution on administration of the clinical study.

Education

Bachelor's degree

Job description

Saint Luke’s Hospital in Kansas City, MO is seeking a Clinical Research Coordinator to join our research team to assist with providing and coordinating care for patients active in various research studies.

You will prepare the site for conduct of the study, identify potential study participants, conduct informed consent, assist with scheduling labs and appointments, gather and record study related data, and provide patient education for various research studies.