Clinical Research Coordinator – GI Trials (Onsite, Aurora)

University of Colorado; South Dakota; Presencial; USD 55.000 - 75.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical insurance

Dental insurance

Retirement 401(a) Plan

Paid time off

Descripción de la vacante

University of Colorado Anschutz Medical Campus seeks an Open Rank Research Services Clinical Research Coordinator to contribute to studies on esophageal disorders. You will join a multidisciplinary team led by principal investigators and GI research leadership, supporting clinical trials and prevention research.

The role involves coordinating trials, ensuring regulatory compliance, and engaging with subjects to obtain consent and data. A collaborative environment with strong benefits is offered.

Formación

• Bachelor's degree in any field (Entry and Intermediate levels).
• One year clinical research or related experience (Preferred qualifications).
• A combination of education and related experience may substitute for a bachelor's degree.

Responsabilidades

• Assist with and oversee day-to-day operations of clinical trials and studies.
• Obtain medical history, medication information, and eligibility for trial participation.
• Conduct informed consent process and ensure proper documentation.
• Interview prospective subjects and educate them on study details.
• Schedule participation and coordinate resources (space, physician, nursing, labs).
• Collect, code, and analyze data accurately and timely.
• Adhere to regulatory standards.
• Other duties as assigned.

Conocimientos

Clinical research experience

Educación

Bachelor's degree in any field

Bachelor's degree in science or health related field

Descripción del empleo

University of Colorado Anschutz Medical Campus seeks an Open Rank Research Services Clinical Research Coordinator to contribute to studies on esophageal disorders. You will join a multidisciplinary team led by principal investigators and GI research leadership, supporting clinical trials and prevention research.

The role involves coordinating trials, ensuring regulatory compliance, and engaging with subjects to obtain consent and data. A collaborative environment with strong benefits is offered.