Clinical Research Coordinator I Non-RN

7 days ago

Denver, Colorado, United States Adventist Health Full time $60,000 - $75,000 per year

All the benefits and perks you need for you and your family:

  • Benefits from Day One 

  • Paid Days Off from Day One 

  • Student Loan Repayment Program 

  • Career Development  

  • Whole Person Wellbeing Resources

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.

Schedule: Full-time

Shift: Days

Location: 2525 S DOWNING ST, Denver, 80210

The role you'll contribute: 

The Clinical Research Coordinator I (CRC I) is involved in all aspects of research conducted including patient screening, assessing eligibility, and coordinating the care and follow-up of volunteers placed on research studies, trials, and programs. Specific activities to include: Research participant recruitment and consenting for the therapeutic areas they serve, provision of concierge level service for all patient facing interactions during the course of clinical trials and research studies, and the coordination of biospecimen collection (i.e. blood, tissue) through collaborative interaction with Clinical Research nursing staff, laboratory teams, hospital departments to ensure ongoing regulatory and protocol compliance. Through collaboration with research assistants and/or clinical coordinators, ensures compliant data entry/data mining into registries, patient records, and research specific database systems. Assists Principal Investigators and research staff in the development of compliant research protocols and other control documents. Serves as the study-specific clinical point of contact for participants, investigators, research staff, hospital departments and external research partners. Actively participates in outstanding customer

The value you'll bring to the team: 

  • Coordinates or performs biospecimen collection and maintains HIPAA-protected databases connecting patient information to biospecimens used in research.

  • Serves as the study-specific point of contact for participants, investigators, research staff, hospital departments, and external research partners.

  • Collaborates with clinical research supervisors and staff to implement standard operating procedures for the Institute's research division.

  • Ensures all patient-facing activities comply with clinical research standards and AHRI procedures.

The expertise and experiences you'll need to succeed:

Required qualifications:

  • Technical/Vocational School, associate, or a bachelor's degree in healthcare administration, research, or related field.

  • 2+ Work Experience

Preferred qualifications:

  • Certified Clinical Research Coordinator (CCRC) Preferred or

  • Certified Clinical Research Professional (SOCRA) (CCRP) Preferred and

  • Basic Cardiac Life Support (BCLS) Preferred

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