Oncology Clinical Research Coordinator - Day Shift

Saint Luke's Health System; Kansas City, Northern (MO, KY); Hybrid; USD 55,000 - 75,000; Full time

Job summary

Saint Luke’s Hospital in Kansas City, MO, is seeking a Clinical Research Coordinator to support oncology research studies. The role includes coordinating study activities, preparing the site for visits, identifying participants, and obtaining informed consent under the supervision of the Principal Investigator.

Requirements include a Bachelor’s degree and the ability to manage multiple tasks and deadlines in a fast-paced research environment.

Qualifications

• Bachelor's degree required.
• Experience in coordinating clinical research activities is preferred (less than 1 year).
• Ability to obtain informed consent and coordinate data collection.

Responsibilities

• Supports, facilitates and coordinates daily clinical trial activities and study conduct.
• Works under the supervision of the Principal Investigator to support compliance, budgeting, and study documentation.
• Prepares the site for study visits, screens potential participants, obtains consent, and schedules labs and visits.

Skills

Clinical Research Coordination

Informed Consent

Study Data Collection

Education

Bachelor's degree

Job description

Saint Luke’s Hospital in Kansas City, MO, is seeking a Clinical Research Coordinator to support oncology research studies. The role includes coordinating study activities, preparing the site for visits, identifying participants, and obtaining informed consent under the supervision of the Principal Investigator.

Requirements include a Bachelor’s degree and the ability to manage multiple tasks and deadlines in a fast-paced research environment.