CLINICAL RESEARCH COORD
Chesterfield, MOFull-time
Behavioral Health Market Context
Apply Nowvia Lensa
Benefits
Health InsurancePaid Time Off
Job Description
lence, 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.
Education, Experience, & Licensing Requirements:
Must have one of the following:
• Nursing Diploma or Associates in Nursing and current licensure as a Registered Nurse in the state of Missouri required
• Previous clinical research experience preferred.
• Bachelor's degree required and 1 year of clinical research-related experience preferred.
• Associate's Degree required and minimum of 2 years clinical research experience preferred.
Benefits for a Better You:
• Day one benefits package
• Pension Plan & 401K
• Competitive compensation
• FSA & HSA options
• PTO programs available
• Education Assistance
Why You Belong Here:
You matter. We could not achieve our mission daily without the hands of our team. Our culture and compassion for our patients and team is a distinct reflection of our dynamic workforce. Each team member is focused on being part of something much bigger than themselves. Join our St. Luke's family to be a part of making life better for our patients, their families, and one another.
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.
Education, Experience, & Licensing Requirements:
Must have one of the following:
• Nursing Diploma or Associates in Nursing and current licensure as a Registered Nurse in the state of Missouri required
• Previous clinical research experience preferred.
• Bachelor's degree required and 1 year of clinical research-related experience preferred.
• Associate's Degree required and minimum of 2 years clinical research experience preferred.
Benefits for a Better You:
• Day one benefits package
• Pension Plan & 401K
• Competitive compensation
• FSA & HSA options
• PTO programs available
• Education Assistance
Why You Belong Here:
You matter. We could not achieve our mission daily without the hands of our team. Our culture and compassion for our patients and team is a distinct reflection of our dynamic workforce. Each team member is focused on being part of something much bigger than themselves. Join our St. Luke's family to be a part of making life better for our patients, their families, and one another.
Qualifications
- •Nursing Diploma or Associates in Nursing and current licensure as a Registered Nurse in the state of Missouri required
Benefits
- •Day one benefits package
- •Pension Plan & 401K
- •Competitive compensation
- •FSA & HSA options
- •PTO programs available
- •Education Assistance
Responsibilities
- •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
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