Hybrid Clinical Research Coordinator

University of Colorado; United States; Hybrid; USD 52,000 - 76,000; Full time

Benefits offered by this job

Health benefits

Dental and vision plans

Retirement plan 401(a) with employer

Job summary

University of Colorado Anschutz Medical Campus, Linda Crnic Institute for Down Syndrome, seeks a Clinical Coordinator to support clinical research and trials with human subjects. This role involves coordinating activities, collecting health data, and assisting with informed consent and regulatory documentation.

You will manage day-to-day trial operations, partner with physicians and staff, and ensure accurate study materials and documentation.

Qualifications

• Entry Level: Bachelor's degree in any field from an accredited institution
• Substitution: A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor's degree on a year for year basis.
• Intermediate Level: Bachelor's degree in any field from an accredited institution
• Substitution: A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor's degree on a year for year basis.
• One (1) year of clinical research or related experience
• Senior Level: Bachelor's degree in any field from an accredited institution
• Two (2) years clinical research or related experience
• Substitution: An advanced degree (Masters or Doctorate) may be substituted for experience on a year for year basis if the degree is in a field of study directly related to the work assignment.
• Applicants must meet minimum qualifications at the time of hire.

Responsibilities

• Perform day-to-day operations of clinical trials and studies
• Obtain medical history from consented participants, including follow-up for off-site medical records and completion of a participant health survey.
• Must be able to reliably transcribe orally reported medical history as written notes.
• Obtain informed consent and/or assent from study participants and ensure that the process is properly documented, and that informed consent form documents are filed as required.
• Schedule subject participation in research clinical trials and coordinate the availability of necessary space and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy).
• Adhere to research regulatory standards.
• Collect code, and summarize information obtained from research in an accurate and timely manner
• Master study materials, including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies

Job description

University of Colorado Anschutz Medical Campus, Linda Crnic Institute for Down Syndrome, seeks a Clinical Coordinator to support clinical research and trials with human subjects. This role involves coordinating activities, collecting health data, and assisting with informed consent and regulatory documentation.

You will manage day-to-day trial operations, partner with physicians and staff, and ensure accurate study materials and documentation.