Clinical Research Coordinator – Open Rank, Renal Trials, Onsite

University of Colorado; Aurora (CO); On-site; USD 54,000 - 69,000; Full time

Benefits offered by this job

Employer contributes 10% to 401(a)

Vacation and sick leave

Tuition benefit

ECO Pass

Holiday leave

Job summary

University of Colorado Anschutz Medical Campus is seeking an Open Rank Research Services Clinical Sciences Professional (Intermediate – Senior) to coordinate a large R01 trial focused on Type 2 Diabetes in adults. The role is onsite in Aurora, CO and involves data management, patient visits, and coordinating with investigators and staff.

Responsibilities include conducting visits, using CTRC Scheduler, transporting supplies, scheduling eye exams, performing vascular testing, and maintaining

Qualifications

• Bachelor’s degree required; one year of clinical research or related experience for intermediate level.
• Senior level requires two years of clinical research or related experience.
• Advanced degree may substitute for experience on a year-for-year basis.
• Knowledge of federal regulations and GCP is preferred.

Responsibilities

• Coordinate and conduct research visits at Adult CTRC.
• Utilize CTRC Scheduler for visit management.
• Transport study supplies and samples across campus.
• Schedule eye exams at Barbara Davis Center when needed.
• Perform vascular testing using the AtCor SphygmoCor.
• Maintain accurate study records and data entry.

Skills

GCP knowledge

Oral and written communication

Customer service

Anatomy knowledge

Research protocol interpretation

Education

Bachelor’s degree in any field

Advanced degree (Masters/PhD) in related field

Tools

EMR/EHR systems

Data management systems

Job description

University of Colorado Anschutz Medical Campus is seeking an Open Rank Research Services Clinical Sciences Professional (Intermediate – Senior) to coordinate a large R01 trial focused on Type 2 Diabetes in adults. The role is onsite in Aurora, CO and involves data management, patient visits, and coordinating with investigators and staff.

Responsibilities include conducting visits, using CTRC Scheduler, transporting supplies, scheduling eye exams, performing vascular testing, and maintaining