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Community Hospital Clinical Research Coordinator, Grand Valley Oncology, Full-Time in Grand Junction, Colorado

The Job: Coordinates the implementation, quality control, and completion of research studies while assisting the Principal Investigator in determining and accomplishing study objectives. Oversees research studies in an administrative and operational capacity while maintaining compliance with guidelines set by policies, oversight and/or governing agencies. Promotes a collaborative, interdisciplinary approach towards patients, families, and all members of the care delivery team in regard to internal and external research projects.

Work Schedule: Full Time

Location: Grand Valley Oncology

Primary Responsibilities:

  • Utilizes knowledge of study protocol, medications, procedures, infection control, safety precaution to initiate appropriate interventions by assisting, coordinating, performing, and/or overseeing all clinical related aspects of assigned research protocols and research subjects.

  • Coordinates and performs responsibilities related to research participants, including determining subject population availability, developing informed consents and screening materials, screening and recruiting subjects, coordinating referrals for external clinical trials, and/or coordinating with referring physicians to provide information regarding available research projects to maintain good communication and a strong referral basis.

  • Develops and maintains patient databases, investigational logs, records of drugs administered, medical devices monitored, and/or procedures followed.

  • Assist with study budgets, coverage analysis and sponsor billing.

  • Assist with preparation, submission and maintenance of IRB, FDA, NCI, NIH, NSF and/or other regulatory documents and research correspondence.


  • Associate or Bachelor?s degree in business, science or related filed.

  • At least (1) year of Oncology Experience (Preferred).

  • At least (1) one year of Research Experience (Preferred).

  • Knowledge of Good Clinical Practices, FDA, HIPAA and IRB regulations, having at least a basic understanding of research procedures.

  • ACRP / SOCRA certification within 6 months of being eligible (SOCRA is preferred);

  • CITI and IATA within 30 days of being hired.

This position's pay range is: $19.43 ? 27.20 per hour, depending on education and experience.

Discretionary bonuses, relocation expenses, merit increases, market adjustments, recognition bonuses and other forms of discretionary compensation may be paid to eligible employees based upon organizational and individual performance.


Employees are eligible to participate in an attractive benefits package including medical, dental, vision, paid time off, education assistance, 403(b) with employer matching, and more. Eligibility is based on employment status. Details regarding specific benefit you may be eligible for will be discussed during the hiring process.

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