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Intermediate Clinical Sciences Coordinator

University of Colorado
Aurora, US
$52K-$66.1K a year
Full-time

Intermediate Clinical Sciences Coordinator-34507University Staff

Description

University of Colorado Anschutz Medical Campus

School of Medicine Department of Medicine Division of Gastroenterology & Hepatology

Job Title : Intermediate Clinical Sciences Coordinator

Position : #00825940 Requisition : #34507

Job Summary :

We are seeking an Intermediate Clinical Sciences Coordinator to join our clinical colorectal cancer screening and prevention research program.

The successful candidate will be part of a team that includes supportive research personnel (regulatory, budget, coordinators) and medical personnel (nurses, genetic counselors, physicians) all led by the principal investigator and the GI division research leadership.

The candidate will participate in clinical research projects including studies examining different colorectal cancer prevention strategies in prospective clinical trials, studies examining the prevalence of genetic syndromes that increase risk of cancer among patients with colorectal polyps, cancer prevention vaccine trials, development of mobile / digital applications to help patients improve cancer prevention care and many more.

The position requires an ability to work independently, but collaboratively, have attention to detail, and be able to maintain organized protocol documentation and data.

Furthermore, the Intermediate Clinical Science Professional will have the opportunity to manage and lead teams. The studies we conduct require in-person and telephone interactions with participants / patients / staff, thus we are seeking a candidate who is a people person and can interact well with others.

Key Responsibilities :

  • Independently master study materials, including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies.
  • Independently perform study related processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies.
  • Assist Team Leads, Supervisors and / or management with creation and implementation of processes and procedures and quality improvement initiatives.
  • Act as a Primary Coordinator on multiple trials / studies.
  • Assist and train junior team members.

Work Location :

Onsite / Hybrid this role is expected to work onsite in Aurora, CO with the potential for a hybrid schedule (3 4 days per week on campus) after evaluation of work after at least 30 days.

Why Join Us

30+ days ago
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