Clinical Research Coordinator I RN

Job Description

Executes and coordinates the informed consent process for participants in clinical trials and research studies.

Screens potential research participants to determine eligibility for clinical trials and studies.

Provides detailed information about the study, including its purpose, procedures, risks, and benefits, to potential participants.

Ensures that participants fully understand the informed consent document before they sign it, and clarifies any questions or concerns.

Maintains accurate and complete records of the informed consent process, including signed consent forms and documentation of discussions.

Knowledge, Skills, And Abilities

• Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice.
• Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner.
• Ability to acclimate and integrate into various clinical settings as needed per protocol.
• Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures.
• Knowledge of HIPAA data protection and patient advocacy or similar awareness of ethical treatment of participants in research.

Education

• Associate's of Nursing [Required]
• Bachelor's of Nursing [Preferred]
• Field Of Study Nursing

Work Experience

• N/A

Additional Information

• N/A

Licenses And Certifications

• Registered Nurse (RN) [Required]
• Basic Life Support - CPR Cert (BLS) [Required]
• Certified Clinical Research Coordinator (CCRC) [Preferred]

Physical Requirements

View Physical Requirements

Pay Range

$65,582.40 - $108,646.85