Clinical Research Coordinator Level 1

BHS • Elizabethtown, KY

10d

About The Position

Baptist Health is hiring a Clinical Research Coordinator Level 1 in Elizabethtown, Kentucky. Under limited supervision, the Clinical Research Coordinator coordinates patient care in compliance with local, state, and federal guidelines and regulations and IRB-approved protocol requirements. The role applies developing or basic clinical trial research knowledge and hospital experience while working collaboratively with individuals involved in patient care and treatment.

The coordinator is expected to build knowledge of the organization, research processes, and scope of work through daily experience, collaboration with senior staff, and seeking learning opportunities. The role involves understanding the guidelines, regulations, and policies for clinical trial research, using that knowledge to evaluate and resolve issues or seek guidance, and coordinating trials according to protocol in collaboration with investigators, research staff, and departmental stakeholders. Clear documentation covers 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.
• Proficiency with computers, including navigating websites, electronic data systems, electronic medical records, Excel, Word, and PowerPoint.
• Must obtain ACLS/BLS training within six months.

Nice To Haves

• Oncology clinical experience is preferred but not required.

Responsibilities

• Coordinate patient care in accordance with local, state, and federal guidelines and regulations and IRB-approved protocol requirements.
• Collaborate with investigators, research staff, departmental stakeholders, and individuals involved in patient care and treatment to coordinate clinical trials according to protocol.
• Document changes in patient condition, adverse events, concomitant medication use, protocol compliance, and responses to study interventions.
• Use knowledge of clinical trial research guidelines, regulations, and policies to evaluate and resolve problems or seek guidance.
• Build knowledge and capabilities related to the organization, research processes, and scope of work through daily experience and collaboration with senior staff.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree