
Urology Clinical Research Coordinator-RN
Denver, COFull-time$72–124K/yrSeen 1w agoSeen in employer's feed 2 days ago
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At a glance
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Requirements
Credentials this posting asks for.
Job overview
The Urology Clinical Research Coordinator-RN executes and coordinates informed consent, participant screening, biospecimen collection, and follow-up for clinical trials and research studies. The role serves as a clinical point of contact for participants and research partners, maintains study records and protected databases, and supports clinical tasks within scope of practice. The posting prefers specialized knowledge of assigned therapeutic areas and one to two years of human life sciences or biomedical research experience.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Our promise to you:
Joining AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better.
All the benefits and perks you need for you and your family:
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Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance
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Paid Time Off from Day One
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403-B Retirement Plan
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4 Weeks 100% Paid Parental Leave
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Career Development
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Whole Person Well-being Resources
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Mental Health Resources and Support
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Pet Benefits
Schedule:
Full time
Shift:
Day (United States of America)
Address:
2525 S DOWNING ST
City:
DENVER
State:
Colorado
Postal Code:
80210
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. Coordinates or performs biospecimen collection and maintains HIPAA protected database connecting patient information to biospecimens used in research. Serves as the study-specific clinical point of contact for participants, investigators, research staff, hospital departments and external research partners. Maintains sensitivity to cost containment measures by conserving hospital supplies and human resources while overseeing proposed project budgets. Conducts research regarding patient screening and clinical eligibility assessments. Coordinates the care and follow-up of volunteers placed on research studies, trials, and programs. Provides ongoing support and information to participants throughout the duration of studies. Works flexible hours and is available for research project-related questions 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 Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures. Other duties as assigned.
Knowledge, Skills, and Abilities:
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Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice. [Required]
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Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner [Required]
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Ability to acclimate and integrate into various clinical settings as needed per protocol [Required]
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Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures. [Required]
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Knowledge of HIPAA data protection and patient advocacy or similar awareness of ethical treatment of participants in research [Required]
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Ability to communicate effectively with research participants, investigators, research staff and external partners. [Required]
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Ability to apply analytical approach to problem solving, obtain and analyze facts, and apply sound judgement. [Required]
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Ability to accept direction and respond to the changing needs of clinical research units [Required]
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Working knowledge of Microsoft Office applications, such as, Word, Excel, Access, Outlook, and Internet knowledge and skill [Required]
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Specialized knowledge of the unique needs of patients in the assigned therapeutic areas undergoing treatment [Preferred]
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Specialized knowledge of assigned therapeutic areas as it relates to research and clinical trials. [Preferred]
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One to two years skill in human life sciences/biomedical research; physiological, cellular, biochemical, or molecular biology [Preferred]
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Bilingual (English/Spanish) [Preferred]
Education:
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Associate's of Nursing [Required]
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Bachelor's of Nursing [Preferred]
Field of Study:
- Nursing
Work Experience:
- N/A
Additional Information:
- N/A
Licenses and Certifications:
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Registered Nurse (RN) [Required]
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Basic Life Support - CPR Cert (BLS) [Required]
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Certified Clinical Research Coordinator (CCRC) [Preferred]
Physical Requirements: (Please click the link below to view work requirements)
Physical Requirements - https://tinyurl.com/msy4mja2
Pay Range:
$71,968.00 - $124,446.40
This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances.
Category: Registered Nurse
Organization: AdventHealth Porter
Schedule: Full time
Shift: Day
Req ID: 154070387
How this job compares
Set against the 603 open Clinical Research Coordinator jobs on Olive Jobs, counted November 2, 2026.
- Pay
- This posting$72–124K/yr
- US median$56–74K/yr154 salary ranges
This range's midpoint, $98K, is 49% above the US median midpoint ($66K) — in the top quarter of Clinical Research Coordinator salary ranges across the US.
- Openings
- Olive Jobs lists 603 open Clinical Research Coordinator jobs across the US. 2% of them nationwide are listed as remote or flexible.
- Hiring the most across the US
- Mount Sinai Health System44 open
- Iterative Health39 open
- University of Miami39 open
- Experience
- Clinical Research Coordinator postings that state a minimum ask for 2 years of experience at the median; the middle half ask for 1 to 3 years (394 postings).
- Education
- This posting asks for an associate degree; 232 of the 603 open Clinical Research Coordinator jobs (38%) ask for an associate degree or higher.
Counted across the open, public US postings on Olive Jobs on November 2, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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