$71,968 – $124,446
Listed on AdventHealth’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
A clinical research coordinator role at a hospital where you'll manage the informed consent process, screen participants for eligibility, and support their ongoing engagement in urology clinical trials. This suits registered nurses with clinical experience who want to transition into research while maintaining direct patient interaction and using their clinical skills.
Our summary, not AdventHealth’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- Registered Nurse license (RN)
- Associate's degree in Nursing
- Basic Life Support / CPR certification
- Ability to perform clinical tasks including assisting with minor procedures within scope of practice
- Work independently in fast-paced clinical and research environments
- Manage multiple tasks simultaneously in an organized manner
- Clinical competencies including physical assessment, phlebotomy, IV insertion, and administration of investigational drugs
- Knowledge of HIPAA and patient advocacy in research ethics
- Effective communication with research participants, investigators, staff, and external partners
- Analytical problem-solving and sound judgment
- Flexibility to acclimate to various clinical settings per protocol
- Working knowledge of Microsoft Office applications
- Coordination of informed consent process and participant screening
Nice to have
- Bachelor's degree in Nursing
- Specialized knowledge of urology or assigned therapeutic area
- Knowledge of assigned therapeutic area as it relates to clinical trials
- One to two years of experience in human life sciences or biomedical research
- Bilingual capability (English/Spanish)
- Certified Clinical Research Coordinator (CCRC) certification