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Senior Clinical Research Coordinator Childrens Oncology

Job in Aurora, Arapahoe County, Colorado, 80012, USA
Listing for: Children's Hospital Colorado
Per diem position
Listed on 2026-01-11
Job specializations:
  • Healthcare
    Clinical Research
Job Description & How to Apply Below

Job Overview

The Clinical Research Coordinator Senior is a seasoned coordinator who can work across multiple complex modalities and is responsible for participating in the day‑to‑day operations of complex, multi‑site clinical research programs and/or studies conducted by Principal Investigators (PIs) at the University of Colorado Anschutz Medical Campus. Performs a variety of administrative and operational duties involved in the collection, compilation, documentation, and review of clinical research data.

Facilitates the accomplishment of research programs and/or study goals. Works independently and leads others in navigating the clinical research environment and participates in a variety of departmental and/or divisional initiatives. Provides oversight to Clinical Research Coordinators and other related team members. Works under minimal supervision.

We are looking for a motivated, detail‑oriented, highly organized, team‑oriented person to join our Children's Oncology Group research team in the Center for Cancer and Blood Disorders (CCBD). The Children’s Oncology Group (COG) is a cooperative group specializing in pediatric clinical research inclusive of children, adolescents and young adults with cancer. The COG partners with research scientists from around the world in efforts to understand the causes of cancer and find more effective treatments for the children we care for.

Today, more than 90% of 16,000 children and adolescents diagnosed with cancer each year in the United States are cared for at Children’s Oncology Group member institutions. COG’s unparalleled collaborative efforts provide the information and support needed to answer important clinical questions in the fight against cancer. The Children’s Oncology Group has nearly 100 active clinical trials open at any given time.

These trials include front‑line treatment for many types of childhood cancers, studies aimed at determining the underlying biology of these diseases, and trials involving new and emerging treatments, supportive care, and survivorship. The Children’s Oncology Group research has turned children’s cancer from a virtually incurable disease 50 years ago to one with a combined 5‑year survival rate of 80% today.

Our extraordinary team at Children’s Hospital Colorado is creating the future of child health, and we need top talent to do it. Join us!

Additional Information

Hours per week: 40, eligible for benefits.

Shift: Monday - Friday, work hours may vary due to department needs. This position may have the possibility of being hybrid upon successful completion of department on‑boarding/training and job performance.

May require occasional weekend and holiday coverage.

Duties & Responsibilities
  • Documentation/Data Collection - Prepares and takes part in site initiation, monitoring, closeout visits, and document storage activities, and related training, creation of SOPs and implementation of operational plans. Assembles the necessary parties to ensure that all required agreements are in place. Utilizes and assists with training team members on electronic data capture systems, technologies, and software necessary for clinical research program and/or study operations.

    Scores tests, enters data, and completes required forms accurately and according to protocol. Leads the development of data collection documents and instruments, maintains subject level documentation, and prepares documents, equipment and/or supplies, identifies issues recommends solutions.

  • Regulatory - Identifies and liaises with various regulatory partners (IRB, compliance, legal) as needed for clarity in effectively supporting research operations. Identifies gaps and participates in policy, standard operating procedures and guideline development as required to enhance research operations in the CHRE. Submits assigned studies for review and approval and provides status updates throughout the startup process. Assists regulatory team with Institutional Review Board (IRB) preparation and submission.

  • Study Participation - Screens, schedules, consents participants in a variety of clinical research programs and/or studies. Explains the difference between clinical…

Position Requirements
10+ Years work experience
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