Clinical Research Coordinator I

Kyeatright; Lexington, Northern (KY, KY); Hybrid; USD 45,000 - 60,000; Full time

Job summary

Baptist Health in Lexington, KY seeks a Clinical Research Coordinator I to coordinate patient care under IRB-approved protocols. Under limited supervision, you will work with investigators and research staff to ensure protocol compliance and proper documentation, while expanding your clinical trial knowledge and organizational skills.

Ideal candidates have a technical degree in a health-related field and at least 3 years of clinical research experience, with proficiency in EMR, Excel, and office

Qualifications

• 3 years of experience in clinical research or as a clinical trial coordinator.
• Proficient with computers, navigating websites and data systems.

Responsibilities

• Coordinate patient care in line with IRB-approved protocols.
• Collaborate with investigators and staff to conduct trial coordination and documentation.

Skills

Clinical research experience

Education

Technical Diploma or Degree in biology/public health/pharmacy/health field

Tools

Excel

Electronic Medical Records

Electronic Data Capture

Word

PowerPoint

EHR

Job description

Clinical Research Coordinator I page is loaded## Clinical Research Coordinator Ilocations: Lexington, KYtime type: Full timeposted on: Posted Yesterdayjob requisition id: R26107977**Summary**See attached**Job Description:*****Baptist Health is looking for a Clinical Research Coordinator I to join our team in Lexington, KY***Under limited supervision, the Clinical Research Coordinator I (CRC) coordinates patient care in compliance with local, state and federal guidelines and regulations through IRB approved protocol requirements. The CRC uses their developing and/or basic knowledge of clinical trial research along with their hospital experience to work collaboratively with individuals associated with the care and treatment of the patient. It is the expectation the CRC will utilize day-to-day experience and collaborations with senior staff to broaden their knowledge base and capabilities. They will seek out opportunities to build their knowledge of the organization, research processes and scope of work. They will understand the guidelines, regulations, and policies associated with conducting clinical trial research and use that insight to evaluate and resolve problems or seek out guidance. The CRC collaborates with the investigators, research staff and other departmental stakeholders to conduct clinical trial coordination per protocol. Through clear documentation, the CRC will define any changes in condition, adverse events, concomitant medication use, protocol compliance, and response to study intervention. The CRC works collaboratively with individuals associated with the care and treatment of the patient.***Qualifications:**** Technical Diploma or Degree/certification must be 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.### *If you would like to be part of a growing family focused on supporting clinical excellence, teamwork and innovation, we urge you to apply now!*### Baptist Health is an *Equal Employment Opportunity* employer.(blob:https://bhs.wd1.myworkdayjobs.com/42a47a07-a597-4529-9deb-9c0499163cb6)0:00 / 2:44