Clinical Research Coordinator I Non-RN
Salary undisclosed
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All the benefits and perks you need for you and your family:
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 Non-RN (CRC I Non-RN) 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
The Expertise And Experiences You’ll Need To Succeed
- Benefits from Day One
- Paid Days Off from Day One
- Student Loan Repayment Program
- Career Development
- Whole Person Wellbeing Resources
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 Non-RN (CRC I Non-RN) 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
- Execute and coordinate the informed consent process for AdventHealth Research Institute (AHRI) in the Rocky Mountain Region (RMR) participants in clinical trials and research studies across multiple locations. This may require travel between sites and research laboratories, and/or the use of technology.
- Responsible for all aspects of research conducted including patient screening, assessing eligibility, and coordinating the participation and follow-up of volunteers placed on research studies, trials, and programs.
- Coordinate research participant recruitment and consenting for the therapeutic areas they serve.
- Provision of concierge level service for all patient facing interactions throughout the course of clinical trials and research studies.
The Expertise And Experiences You’ll Need To Succeed
- Bachelor’s degree in Healthcare Administration, Research, or related field with no experience OR
- Associates degree in Healthcare Administration, Research, or related field and two (2) years’ experience OR
- Graduate of an accredited allied health certificate program with four (4) years of clinical research or healthcare experience.