Clinical Research Coordinator

About This Role

This Clinical Research Coordinator I position coordinates patient care in compliance with local, state, and federal guidelines and regulations through IRB approved protocol requirements. The role involves working collaboratively with individuals associated with the care and treatment of patients, utilizing developing knowledge of clinical trial research and hospital experience.

Responsibilities

• Coordinate patient care in compliance with local, state, and federal guidelines and regulations through IRB approved protocol requirements
• Work collaboratively with individuals associated with the care and treatment of the patient
• Utilize day-to-day experience and collaborations with senior staff to broaden knowledge base and capabilities
• Seek out opportunities to build knowledge of the organization, research processes, and scope of work
• Understand the guidelines, regulations, and policies associated with conducting clinical trial research
• Use insight to evaluate and resolve problems or seek out guidance
• Collaborate with investigators, research staff, and other departmental stakeholders to conduct clinical trial coordination per protocol
• Define any changes in condition, adverse events, concomitant medication use, protocol compliance, and response to study intervention through clear documentation

Requirements

• Technical Diploma or Degree/certification in biology, public health, pharmacy, or health related field
• 3 years of experience in clinical research or as a clinical trial coordinator
• Proficient with a computer including navigating websites, electronic data systems, electronic medical records, Excel, Word, PowerPoint

About the Company

Baptist Health is looking for a Clinical Research Coordinator I to join their team in Lexington, KY.