Clinical Research Coordinator I

Baptist Health; Lexington (KY); On-site; USD 48,000 - 64,000; Full time

Job summary

Baptist Health in Lexington, KY is seeking a Clinical Research Coordinator I to join our team. Under limited supervision, the CRC coordinates patient care in compliance with local, state and federal guidelines through IRB approved protocol requirements.

The CRC collaborates with investigators and staff to manage documentation, adverse events, protocol compliance, and changes in patient condition, building knowledge of the organization and research processes.

Qualifications

• Technical diploma or degree in biology, public health, pharmacy, or health-related field.
• 3 years of experience in clinical research or as a clinical trial coordinator.
• Proficient with Excel, Word, PowerPoint and EMR/electronic data systems.

Responsibilities

• Coordinate patient care under protocol requirements.
• Ensure compliance with IRB and regulatory guidelines.
• Document changes in condition, adverse events, and protocol deviations.
• Collaborate with investigators, research staff, and departmental stakeholders.

Skills

Clinical research

EMR systems

Excel

Word

PowerPoint

Education

Biology/Health field degree

Tools

EMR software

Data entry

Job description

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 inbiology, 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.
  

Baptist Health is an Equal Employment Opportunity employer.