Clinical Research Coordinator - Lung Research Center

St. Luke's Hospital - MO•Chesterfield, MO

2d•Onsite

About The Position

We are dedicated to providing exceptional care to every patient, every time. St. Luke’s Hospital is a value-driven award-winning health system that has been nationally recognized for its unmatched service and quality of patient care. Using talents and resources responsibly, we provide high quality, safe care with compassion, professional excellence, and respect for each other and those we serve. Committed to values of human dignity, compassion, justice, excellence, and stewardship St. Luke’s Hospital for over a decade has been recognized for “Outstanding Patient Experience” by HealthGrades. Position Summary: The primary responsibility of the Clinical Research Coordinator is to manage all aspects of conducting clinical trials under the direction of the Principal Investigator. The Research Coordinator is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As the primary resource for the protocols, the Research Coordinator will act as liaison between the investigators, primary care providers, the institutional review board (IRB) and the sponsor. Along with the investigator, the Research Coordinator will screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, the Coordinator is responsible for all data and source documentation, adverse experience reporting and maintenance of complete regulatory files. Responsible for promoting teamwork with all members of the healthcare team. Performs duties in a manner consistent with St. Luke’s mission and values.

Requirements

Nursing Diploma or Associates in Nursing and current licensure as a Registered Nurse in the state of Missouri required
Previous clinical research experience OR oncology nursing experience required
Bachelor's degree in health-related field and at least 3-5 years of clinical research-related experience
Master’s degree in a related field or 2 years clinical research-related experience

Responsibilities

Manage all aspects of conducting clinical trials under the direction of the Principal Investigator.
Act as liaison between the investigators, primary care providers, the institutional review board (IRB) and the sponsor.
Screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.
Responsible for all data and source documentation, adverse experience reporting and maintenance of complete regulatory files.
Responsible for promoting teamwork with all members of the healthcare team.