Onsite Clinical Research Coordinator - Diabetes Trial Lead

CU Denver; Aurora (CO); On-site; USD 54,000 - 69,000; Full time

Benefits offered by this job

Tuition Benefit

ECO Pass

Paid Time Off

Job summary

The University of Colorado Anschutz Medical Campus in Aurora, Colorado, invites applications for an Open Rank Research Services Clinical Sciences Professional (Intermediate - Senior) to coordinate a large R01 trial on Type 2 Diabetes in Adults.

Primary duties include coordinating research visits, utilizing CTRC Scheduler, transporting study materials, scheduling eye exams, performing vascular testing, and maintaining accurate study records and data entry. Onsite work required.

Qualifications

• Bachelor's degree in any field.
• One year of clinical research or related experience.
• Senior level: Two years of clinical research or related experience.
• Knowledge of federal regulations and Good Clinical Practice (GCP).
• Ability to communicate effectively, both in writing and orally.
• Ability to establish and maintain effective working relationships with employees at all levels.
• Outstanding customer service skills.
• Knowledge of basic human anatomy, physiology, and medical terminology.
• Ability to interpret and master complex research protocol information.

Responsibilities

• Coordinating and conducting research visits at Adult CTRC.
• Utilizing CTRC Scheduler.
• Transport study supplies and samples across campus in timely and safe manner.
• Scheduling eye exams at the Barbara Davis Center.
• Performing vascular testing using the AtCor SphygmoCor.
• Maintaining accurate and up-to-date study records and data entry.

Skills

GCP knowledge

Regulatory compliance

Communication skills

Relationship building

Clinical research experience

Education

Bachelor's degree in any field

Tools

CTRC Scheduler

Job description

The University of Colorado Anschutz Medical Campus in Aurora, Colorado, invites applications for an Open Rank Research Services Clinical Sciences Professional (Intermediate - Senior) to coordinate a large R01 trial on Type 2 Diabetes in Adults.

Primary duties include coordinating research visits, utilizing CTRC Scheduler, transporting study materials, scheduling eye exams, performing vascular testing, and maintaining accurate study records and data entry. Onsite work required.