Clinical Research Coordinator I Non-RN

Adventist HealthDenver, CO
84d

About The Position

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 service.

Requirements

  • Technical/Vocational School, associate, or a bachelor’s degree in healthcare administration, research, or related field.
  • 2+ years of work experience.

Nice To Haves

  • Certified Clinical Research Coordinator (CCRC) Preferred
  • Certified Clinical Research Professional (SOCRA) (CCRP) Preferred
  • Basic Cardiac Life Support (BCLS) Preferred

Responsibilities

  • Research participant recruitment and consenting for the therapeutic areas served.
  • Provision of concierge level service for all patient-facing interactions during clinical trials and research studies.
  • Coordination of biospecimen collection (i.e. blood, tissue) through collaboration with Clinical Research nursing staff, laboratory teams, and hospital departments.
  • Ensuring ongoing regulatory and protocol compliance.
  • Compliant data entry/data mining into registries, patient records, and research-specific database systems.
  • Assisting Principal Investigators and research staff in the development of compliant research protocols and other control documents.
  • Serving as the study-specific clinical point of contact for participants, investigators, research staff, hospital departments, and external research partners.

Benefits

  • Benefits from Day One
  • Paid Days Off from Day One
  • Student Loan Repayment Program
  • Career Development
  • Whole Person Wellbeing Resources

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Education Level

Bachelor's degree

Number of Employees

5,001-10,000 employees

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