Clinical Research Coordinator Hybrid (Down Syndrome)

University of Colorado; Aurora (CO); Hybrid; USD 52,000 - 90,000; Full time

Benefits offered by this job

Medical plans

Dental plans

Retirement 401(a)

Paid time off

Vacation 22 days/year

Sick days 15/year

Holiday days 15/year

Tuition benefit

ECO Pass

Job summary

University of Colorado Anschutz Linda Crnic Institute for Down Syndrome seeks a Clinical Coordinator to manage day-to-day clinical research tasks, obtain histories, and coordinate trial activities. The role emphasizes regulatory compliance and accurate documentation within a hybrid work model.

The position requires a Bachelor's degree with experience in clinical research and familiarity with IRB processes, REDCap, and EDC systems.

Qualifications

• Bachelor’s degree in any field required.
• One year of clinical research or related experience preferred (varies by level).
• Experience with regulatory documentation and IRB processes is beneficial.
• Knowledge of Good Clinical Practice (GCP) and regulatory standards.
• Experience with electronic data capture systems (e.g., REDCap, EDC) recommended.

Responsibilities

• Oversee day-to-day operations of clinical trials and studies.
• Obtain medical history and document informed consent.
• Coordinate scheduling and availability of study resources.
• Adhere to regulatory standards and ensure documentation is complete.
• Assist with study materials and regulatory filings as needed.

Skills

Clinical research

IRB oversight

GCP

Data management

Regulatory submissions

Communication

Spanish beneficial

Education

Bachelor’s degree

Advanced degree substitute

Tools

REDCap

EDC systems

EMR/EHR

Job description

University of Colorado Anschutz Linda Crnic Institute for Down Syndrome seeks a Clinical Coordinator to manage day-to-day clinical research tasks, obtain histories, and coordinate trial activities. The role emphasizes regulatory compliance and accurate documentation within a hybrid work model.

The position requires a Bachelor's degree with experience in clinical research and familiarity with IRB processes, REDCap, and EDC systems.