U

University of Washington

Public research university in Seattle, WA

Lead Clinical Trials Specialist - Multiple Teams

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeSeattle, WA, USA$78.6k - $102k /yrHybrid

About the Job

Requirements

  • A bachelor's degree in a related field and four years of relevant experience; equivalent education and/or experience may substitute unless legal requirements apply.
  • Experience with budget development, clinical research coordination, related project management, or health care.
  • Ability to work and communicate effectively with groups and all levels of faculty, management, and clinical research staff.
  • Organizational and customer service skills.
  • Attention to detail and ability to multitask, organize, and prioritize multiple projects independently.
  • Written and verbal presentation skills.
  • Ability to explain complex policy, financial, and scientific or technical information to a wide audience.
  • Ability to teach and mentor others in group settings, one-on-one sessions, and remotely.
  • Computer skills, including competency with Microsoft Office.
  • Ability to adjust to changing priorities and projects while maintaining a professional demeanor, including in stressful situations.
  • Applicants who have not completed training for clinical research involving human subjects must complete it within 30 days of hire.

Responsibilities

  • Establish and maintain methods for initiating study start-up budgets and implementation planning, delegating tasks, and forecasting start-up workloads.
  • Apply clinical research, medical terminology, and clinical process knowledge to translate oncology protocol requirements into clinical trial budgets and facilitate compliance-office submissions.
  • Work with program leadership and faculty to ensure appropriate study start-up pricing and budget efforts are recorded in study tracking.
  • Negotiate clinical trial budgets and payment terms with study sponsors according to program requirements.
  • Guide regulatory staff on timing submissions to the Scientific Review Committee, UW Human Subjects Division, Radiation Safety, the FDA, and institutional review boards to meet projected start-up deadlines.
  • Coordinate and communicate with UW and Fred Hutch offices involved in clinical trial budget and contract review and negotiation, including the UW Clinical Trial Office, UW Office of Sponsored Programs, and Fred Hutch Clinical Research Support office.
  • Prepare and submit eGC1s according to Clinical Trial Office requirements and deadlines.
  • Ensure significant financial interest compliance is completed and required approvals are received by Clinical Trial Office deadlines.
  • Create Advanced Budget Numbers and work tags.
  • Assist research and finance program managers with developing and communicating study start-up metrics and goals.
  • Forecast, track, and report study start-up timelines.
  • Produce monthly and quarterly study start-up metric reports using established formats.
  • Coordinate with UW and Fred Hutch offices and clinical areas to arrange clinical services and orders.
  • Review protocol amendments and new study materials for changes affecting billing, budgets, research orders, and clinical and financial implementation.
  • Process budget and contract amendments and order changes through UW and Fred Hutch systems.
  • Coordinate with the regulatory team to implement amendments and new study documents.
  • Negotiate clinical trial budget amendments and payment terms with funders.
  • Create new eGC1s and budgets as required by UW Office of Sponsored Programs policies.
  • Assist in hiring and training clinical trials specialists and other start-up and budget-development staff.
  • Provide subject-matter expertise and technical guidance.
  • Work with program leadership to review workloads and delegate tasks.
  • Track workloads and timelines and report findings to program leadership.
  • Work with program leadership to identify process improvements in subject tracking and charge capture.
  • Collaborate with program leadership to address internal budget and subject-tracking audit findings.
  • Develop and manage guidelines that standardize start-up, amendment, and implementation workflows.
  • Perform other related duties as assigned.
  • Work on-site at Fred Hutch Cancer Center and make workday visits to local affiliate locations as required.

Desired Qualifications

  • Experience as a research study coordinator in an academic medical center and/or in oncology clinical research.
  • Familiarity with interpreting regulatory and contractual documents, identifying and resolving ambiguities, negotiating pricing and payment terms, and interpreting complex research-protocol implications.
  • Knowledge of the Medicare Clinical Trials Policy and other federal, state, and institutional clinical research regulations.
  • Experience with REDCap, clinical trial management systems, UW SAGE, and Epic.

About the Company

University of Washington

Public research university in Seattle, WA

The University of Washington is a public research university founded in 1861, with campuses in Seattle, Bothell, and Tacoma. It provides undergraduate, graduate, and professional education alongside research and public service.

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