Clinical Research Coordinator II

AdventHealth • Celebration, FL

405d

About The Position

The Clinical Research Coordinator II (CRC II) at AdventHealth Celebration plays a vital role in the AdventHealth Research Institute (AHRI) by planning, coordinating, and evaluating nursing care for research participants. This position involves adhering to clinical trial protocols, FDA regulations, and ICH/GCP guidelines while advocating for patient rights and safety. The CRC II collaborates with Principal Investigators and other research staff to ensure the integrity and quality of clinical trials.

Requirements

• Bachelor's Degree and 2 years of experience in clinical research, or
• Associates degree and 4 years of experience in clinical research or related field, or
• Graduate of an accredited allied health certificate program with six years of clinical research or healthcare experience.

Nice To Haves

• Master's degree in Healthcare, Research or related field
• Experience in area of specialty as assigned
• Certified Clinical Research Coordinator (CCRC)
• American Heart Association Basic Life Support (BLS) certification
• American Heart Association Advanced Cardiovascular Life Support (ACLS) certification
• Other relevant certifications (e.g., medical assistant, medical technician, phlebotomy)

Responsibilities

• Plan, coordinate, evaluate, and perform nursing care for research participants.
• Collect and manage data for assigned research projects following study protocols.
• Communicate effectively with Principal Investigators, Sub-Investigators, and clinical research support staff.
• Review informed consent documents with study candidates and ensure patient advocacy throughout the trial process.
• Manage multiple clinical trial protocols and ensure accurate documentation and record-keeping.
• Advise Principal Investigators and supervisors of any deviations in trial conduct or patient status.
• Coordinate the work of support staff and laboratory technicians to ensure adherence to research protocols.
• Serve as a liaison between Principal Investigators and the Institutional Review Board (IRB).
• Prepare and review documentation for clinical research study initiation and modifications.
• Assist site monitors during their visits and maintain compliance with regulatory requirements.

Benefits

• Paid Days Off from Day One
• Student Loan Repayment Program
• Career Development
• Whole Person Wellbeing Resources
• Mental Health Resources and Support
• Pet Insurance
• Debt-free Education (Certifications and Degrees without out-of-pocket tuition expense)

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Hospitals
• Education Level: Associate degree