Tissue Bank Coordinator — Clinical Research (Open Rank)

University of Colorado Anschutz; Aurora (CO); In loco; USD 52.000 - 74.000; Tempo pieno

Vantaggi offerti da questo lavoro

Medical: Multiple plan options

Dental: Multiple plan options

Disability, Life, Vision insurance

401(a) Employer retirement plan

Paid Time Off

Vacation days

Sick days

Holiday days

Tuition benefit

ECO Pass

Descrizione del lavoro

University of Colorado Anschutz Medical Campus seeks a Tissue Bank Coordinator to perform clinical research-related tasks, including subject screening, consent documentation, and data handling. The role supports various studies within the Department of Medicine, Division of Hematology, with in-person duties and after a probationary period performance-based flexibility.

The position requires a bachelor’s degree with experience in clinical research, regulatory compliance, and data capture systems.

Competenze

• Bachelor's degree required or substitute education/experience on a year-for-year basis.
• 1 year of clinical research or related experience at minimum.
• Two years of clinical research or related experience for senior level.
• Preferred: three years of clinical research or related experience.
• Experience with electronic data capture systems (EMR/EHR) and data management systems.

Mansioni

• Obtain medical history and current medications; assess eligibility.
• Ensure informed consent process is documented and filed.
• Interview prospective subjects and educate about the study.
• Schedule participation and coordinate clinical support and spaces.
• Maintain study records and CRFs; ensure accuracy and completeness.
• Report adverse events to PI, sponsor, FDA, and DSMC.
• Serve as contact for ongoing studies and onboarding of staff.

Conoscenze

Clinical research

GCP knowledge

Effective communication

Team collaboration

Attention to detail

Regulatory compliance

Formazione

Bachelor's degree in any field

Descrizione del lavoro

University of Colorado Anschutz Medical Campus seeks a Tissue Bank Coordinator to perform clinical research-related tasks, including subject screening, consent documentation, and data handling. The role supports various studies within the Department of Medicine, Division of Hematology, with in-person duties and after a probationary period performance-based flexibility.

The position requires a bachelor’s degree with experience in clinical research, regulatory compliance, and data capture systems.