Clinical Research Coordinator Level 1
About The Position
Baptist Health is seeking a Clinical Research Coordinator Level 1 in Elizabethtown, Kentucky. Under limited supervision, the coordinator coordinates patient care in compliance with local, state, and federal guidelines and regulations and IRB-approved protocol requirements. The role uses developing or basic clinical trial research knowledge and hospital experience to collaborate with people involved in patient care and treatment. The coordinator is expected to expand their knowledge and capabilities through day-to-day experience and collaboration with senior staff, and to seek opportunities to learn about the organization, research processes, and scope of work. The role involves understanding the guidelines, regulations, and policies for clinical trial research and applying that understanding to evaluate and resolve problems or seek guidance. The coordinator works with investigators, research staff, and departmental stakeholders to coordinate clinical trials according to protocol. Clear documentation is used to record changes in patient condition, adverse events, concomitant medication use, protocol compliance, and response to study intervention.
Requirements
- Technical diploma, degree, or certification in biology, public health, pharmacy, or a health-related field.
- Three years of experience in clinical research or as a clinical trial coordinator.
- Computer proficiency, including navigating websites and using electronic data systems, electronic medical records, Excel, Word, and PowerPoint.
- Obtain ACLS/BLS training within six months.
Nice To Haves
- Oncology clinical experience is preferred but not required.
Responsibilities
- Coordinate patient care according to IRB-approved protocol requirements and applicable local, state, and federal guidelines and regulations.
- Collaborate with individuals involved in the patient's care and treatment.
- Work with investigators, research staff, and departmental stakeholders to coordinate clinical trials according to protocol.
- Document changes in patient condition, adverse events, concomitant medication use, protocol compliance, and response to study intervention.
- Use clinical trial research guidelines, regulations, and policies to evaluate and resolve problems or seek guidance.
- Build knowledge of the organization, research processes, and scope of work through experience and collaboration with senior staff.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
