Clinical Research Coordinator - GI Trials & Esophageal Disorders

University of Colorado Anschutz; Aurora (CO); In loco; USD 55.000 - 75.000; Tempo pieno

Descrizione del lavoro

University of Colorado Anschutz Medical Campus seeks an Open Rank Research Services Clinical Research Coordinator to support esophageal disorder studies within the GI division. You will work with a multidisciplinary team to advance clinical trials, manage regulatory documentation, and collect data from adult participants.

The role is onsite in Aurora, CO, with responsibilities spanning subject screening, consent, data management, and coordination with physicians, nurses, and other study staff.

Competenze

• Bachelor's degree required or equivalent experience.
• Experience with clinical research and regulatory standards.
• Familiarity with GCP and regulatory guidelines preferred.
• Strong organizational skills and attention to detail.
• Experience with EMR/EHR and data management systems advantageous.

Mansioni

• Assist with day-to-day operations of clinical trials and studies.
• Obtain subjects' medical history and eligibility; confirm criteria.
• Administer informed consent and ensure proper documentation.
• Schedule subject participation and coordinate clinical trial resources.
• Collect, code, and analyze data accurately; ensure timely reporting.
• Adhere to research regulatory standards and procedures.

Conoscenze

Communication skills

Attention to detail

Team collaboration

Regulatory knowledge

Formazione

Bachelor's degree (any field)

Preferred: Bachelor's degree in science or health related field

Strumenti

EMR/EHR systems

Data management systems

Descrizione del lavoro

University of Colorado Anschutz Medical Campus seeks an Open Rank Research Services Clinical Research Coordinator to support esophageal disorder studies within the GI division. You will work with a multidisciplinary team to advance clinical trials, manage regulatory documentation, and collect data from adult participants.

The role is onsite in Aurora, CO, with responsibilities spanning subject screening, consent, data management, and coordination with physicians, nurses, and other study staff.