Texas Health Huguley FWS
Clinical Research Coordinator I Non-RN
Texas Health Huguley FWS, Denver, Colorado, United States, 80285
Job Description
Clinical Research Coordinator I Non-RN (25040925) Job Number
25040925 Overview
Clinical Research Coordinator I (CRC I) is involved in all aspects of research including patient screening, eligibility assessment, and coordination of care and follow‑up of volunteers placed on research studies, trials, and programs. Schedule
Full‑time | Days Benefits
Benefits from Day One Paid Days Off from Day One Student Loan Repayment Program 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. Role you’ll contribute
Specific activities to include: Research participant recruitment and consenting for therapeutic areas, provision of concierge level service for all patient‑facing interactions during clinical trials and research studies, and 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. 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. Qualifications
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 Certified Clinical Research Professional (SOCRA) (CCRP) Preferred Basic Cardiac Life Support (BCLS) Preferred
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Clinical Research Coordinator I Non-RN (25040925) Job Number
25040925 Overview
Clinical Research Coordinator I (CRC I) is involved in all aspects of research including patient screening, eligibility assessment, and coordination of care and follow‑up of volunteers placed on research studies, trials, and programs. Schedule
Full‑time | Days Benefits
Benefits from Day One Paid Days Off from Day One Student Loan Repayment Program 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. Role you’ll contribute
Specific activities to include: Research participant recruitment and consenting for therapeutic areas, provision of concierge level service for all patient‑facing interactions during clinical trials and research studies, and 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. 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. Qualifications
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 Certified Clinical Research Professional (SOCRA) (CCRP) Preferred Basic Cardiac Life Support (BCLS) Preferred
#J-18808-Ljbffr