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Open Rank Clinical Research Coordinator (Entry - Intermediate)

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University of Colorado Anschutz Medical Campus

13001 E 17th Pl, Aurora, CO 80045, USA

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Open Rank Clinical Research Coordinator (Entry - Intermediate)

Open Rank Clinical Research Coordinator (Entry - Intermediate)

University of Colorado Anschutz Medical Campus

Department: Medicine - Division of Endocrinology, Metabolism, and Diabetes

Job Title: Open Rank Clinical Research Coordinator (Entry - Intermediate)

Position #: 00845601 - Requisition #: 39110

Job Summary:

Under the supervision of the Clinical Research Manager, the primary responsibility of the Entry or Intermediate Clinical Sciences Professional is to serve as a Clinical Research Coordinator in support of various research activities within Dr. Neda Rasouli's Research Program at the University of Colorado Anschutz Medical Campus.

Key Responsibilities:

  • Trial Operations & Management: Assist with and oversee day-to-day operations for multiple clinical trials, acting as the Primary Coordinator to ensure all study activities align with the established protocol.
  • Subject Recruitment & Screening: Participate and lead recruitment efforts by interviewing prospective subjects, reviewing medical histories against inclusion/exclusion criteria, and confirming final eligibility.
  • Informed Consent Oversight: Execute and document the informed consent process, ensuring all participants are fully educated on study details and that legal documentation is filed per regulatory standards.
  • Protocol Execution: Perform study-related procedures, assessments, and drug administrations as defined in the research protocol and in compliance with governing bodies.
  • Subject Scheduling & Coordination: Manage the logistics of subject participation, including the coordination of clinic space and multidisciplinary support (Radiology, Pharmacy, Lab, and PIs).
  • Clinical Assessments: Perform technical clinical tasks including phlebotomy (venipuncture), specimen processing/shipping, EKGs, and monitoring vital signs.
  • Data Management: Abstract, code, and record patient data into Case Report Forms (CRFs) and clinical trial databases with a focus on accuracy and timely entry.
  • Regulatory Compliance: Maintain meticulous study records to ensure strict adherence to FDA guidelines, Good Clinical Practice (GCP), and hospital Standard Operating Procedures (SOPs).
  • Safety Reporting: Promptly alert Principal Investigators, sponsors, and the FDA regarding Serious Adverse Events (SAEs) to ensure patient safety and data integrity.
  • Leadership & Quality Improvement: Assist in the creation of new clinical processes and quality initiatives while training junior staff members on study protocols.

Work Location:

Onsite - this role is expected to work onsite and is located in Aurora, Colorado.

Why Join Us:

The Division of Endocrinology, Metabolism and Diabetes on the state-the-art Anschutz Medical Campus. Our mission is to improve overall health and well-being by prevention, diagnosis, treatment and cure of Diabetes, Obesity, Metabolic disorders and Endocrine disorders through:

  • Cutting-edge basic, translational and clinical research
  • Nationally recognized consultative services in Endocrinology, Metabolism and Diabetes
  • National leadership
  • Training of future leaders in Academic Endocrinology

To learn more about us, please visit: https://medschool.cuanschutz.edu/endocrinology

Qualifications:

Minimum Qualifications:

Entry Level:

  • Bachelor's degree in science or health related field.

Intermediate Level:

  • Bachelor's degree in science or health related field.
  • One (1) year clinical research or related experience.

Applicants must meet minimum qualifications at the time of hire.

Preferred Qualifications:

  • Two (2) years clinical research or related experience.

Knowledge, Skills, and Abilities:

  • Ability to communicate effectively, both in writing and orally.
  • Ability to establish and maintain effective working relationships with employees at all levels throughout the institution.
  • Knowledge of basic human anatomy, physiology, and medical terminology.
  • An understanding of genetics and molecular genetics.
  • Ability to interpret and master complex research protocol information.
  • Excellence with computer skills with Microsoft Office, including Word, Excel, PowerPoint and Outlook.
  • Knowledge of the research process, e.g., research protocols, surveys.

Anticipated Pay Range:

  • Entry Level: $48,446 - $55,000
  • Intermediate Level: $52,721 - $60,000
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