Lead Clinical Research Coordinator

St. Luke's Hospital•Chesterfield, MO

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: Position oversees and coordinates complex clinical research studies. Facilitates and maintains effective and positive working relationships with patients, sponsors, physicians, and employees. Assists with training new research team members; acts as a resource and provides support to research staff to ensure trial processes and procedures are completed as specified in the protocol. Implements and coordinates all phases of study protocols; ensures compliance with protocol guidelines and requirements of regulatory agencies; identifies problems and/or inconsistencies and monitors participant’s progress to include documentation and reporting of adverse events. Develops opportunities for quality improvement in the research process and assists with creation of standard operating procedures. Assist with study start up activities and contract and budget preparation. 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 Degree with active nursing license and 1 year of research experience.
Bachelors in Health related field and 3-5 years of research experience.
Current licensure as a Registered Nurse in the state of Missouri
CPR Certification

Responsibilities

Oversees and coordinates complex clinical research studies.
Facilitates and maintains effective and positive working relationships with patients, sponsors, physicians, and employees.
Assists with training new research team members
Acts as a resource and provides support to research staff to ensure trial processes and procedures are completed as specified in the protocol.
Implements and coordinates all phases of study protocols
Ensures compliance with protocol guidelines and requirements of regulatory agencies
Identifies problems and/or inconsistencies and monitors participant’s progress to include documentation and reporting of adverse events.
Develops opportunities for quality improvement in the research process and assists with creation of standard operating procedures.
Assist with study start up activities and contract and budget preparation.
Responsible for promoting teamwork with all members of the healthcare team.
Performs duties in a manner consistent with St. Luke’s mission and values.