Clinical Research Coordinator I

Baptist Health System, Inc.; Lexington (KY); On-site; USD 52,000 - 70,000; Full time

Job summary

Baptist Health in Lexington, KY is seeking a Clinical Research Coordinator I to coordinate patient care in IRB-approved trials and ensure protocol compliance.

Under limited supervision, you will collaborate with investigators and research staff, manage documentation of adverse events and protocol changes, and contribute to the trial's overall success in a hospital setting.

Qualifications

• Requires technical diploma or degree in biology, public health, pharmacy, or health-related field.
• At least 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.

Responsibilities

• Coordinate patient care per IRB-approved protocol.
• Collaborate with investigators and departmental staff to conduct trial activities.
• Document changes in condition, adverse events, and protocol compliance.

Skills

Clinical research experience

Education

Technical Diploma or Degree in biology, public health, pharmacy, or health related field

Tools

EMR systems

Excel

Word

PowerPoint

Web navigation

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.