Career Opportunities

Coverage Analysis Supervisor at University of California San Francisco

Posted on October 6, 2020 by Patrick Oh

The Coverage Analyst Supervisor provides oversight of team processes and workflow, develops and maintains a thorough training program, and oversees a rigorous quality control program. The individual serves as a technical expert and adviser to the Manager. The Coverage Analyst Supervisor ensures coverage analyses are compliant with all relevant regulations and serves as the internal first-line contact for compliance issues. The individual is responsible for writing SOPs and ensuring analysts are adhering to policies and procedures. The Coverage Analyst Supervisor works collaboratively with Principal Investigators, project managers, study coordinators, budget analysts, and other research staff. The individual tracks key metrics, monitors timelines, and develops efficient workflows. The Coverage Analyst Supervisor evaluates business processes for operational and financial effectiveness. The individual is responsible for hiring and retaining staff, managing work assignments, and performance management.

Patrick Oh
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CTMS Calendar Builder at University of Colorado, Anschutz Medical Campus

Posted on September 21, 2020 by Amanda Childs

This position works within the Clinical Research Administration Office (CRAO) and in collaboration with the Colorado Clinical Translational Science Institute. CRAO is seeking a full-time clinical trials Calendar Builder at the Anschutz Medical Campus. As a key member of the finance and clinical research support team, this position works extensively with budget specialists, clinical research coordinators, principal investigators, various stakeholders of the University of Colorado Cancer Center, University and University of Colorado affiliates, to assist with building of calendars in accordance with budgets in the OnCore Clinical Trials Management System (CTMS). This position will be responsible for the ongoing support of the calendar and budget build functions in OnCore.

Full job description can be found at CU Careers website (, position number 17053

Amanda Childs

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Business Systems Analyst – Research Administration at University of Colorado Denver

Posted on September 16, 2020 by Marissa Macri

This is a Full-time (40 hrs/wk), Salaried/Exempt position on UCHealth’s Research Administration team based on the Anschutz Medical Campus in Aurora, Colorado.

Identifies user needs to determine and implement systems that will meet business requirements. Writes high-level design specifications for users and programmer/analysts. Works with others to determine effective and efficient methods of implementing applications. Designs, codes and tests applications following departmental standards.

Job Duties
– Works with users to determine business needs which may be met through the use of eConsent support, Epic ULearns, Epic Optimization, and Customer service experience
• equests, Tipsheet creation, and EHR requests
• Designs and develops detailed reports according to user needs using structured design, and responds to user needs as appropriate.
• Analyzes work flow to determine best application with the system. Assists in modifying the user workflow to optimize the system usage. Partners with users for seamless transition to using the application.
• Manages QA projects in department related to the use of the Clinical Trials Management System (OnCore) and the Electronic Health Record (Epic). Works on post OTA activation in OnCore, CMP creation and maintenance, and amendment timelines.

Marissa Macri

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Clinical Trial and Data Management Research Manager at University of Iowa Holden Comprehensive Cancer Center

Posted on September 15, 2020 by Cena Jones-Bitterman, MPP, CIP

To coordinate and manage clinical trial regulatory activities within the Clinical Research Services (CRS) of Holden Comprehensive Cancer Center (HCCC):

  • Oversees clinical research regulatory workflow processes.
  • Develops/maintains a dynamic process to move studies efficiently through Confidentiality
    Disclosure Agreement (CDA) workflows.
  • Continuously evaluates existing procedures for documenting regulatory processes to
    determine and implement methods to improve efficiency and accuracy.
  • Develops and recommends short and long-term program objectives and strategies for
    process improvement implementation.
  • Participates in committees, making recommendations, voting, and implementing change as
  • Assists in orientation and education of new staff and faculty regarding the clinical trial
    regulatory process and expectations.

For a complete description please refer to req# 20002557 at jobs@uiowa

Sanela Krdzic
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About the Career Opportunity Listing

The career opportunities listed here are submitted by members of Onsemble.

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