Senior Oncology Clinical Research Lead

The START Center for Cancer Research

West Valley City (UT)

On-site

USD 85,000 - 110,000

Full time

28 hours ago
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Benefits offered by this job

401(k) retirement savings with company
Annual performance bonus
Generous paid time off

Job summary

The START Center for Cancer Research is seeking a Supervisor, Research Coordinator to lead the Clinical Research Coordinator team and ensure study conduct complies with GCP and START standards. You will collaborate with Nursing, Data Coordination, and Shared Services to support clinic operations, study activation, and quality activities.

The role emphasizes staff training, workload planning, and performance oversight in an oncology-focused environment, with regular M-F hours and fixed site

Qualifications

  • Associate’s degree in health administration, nursing, or related field required.
  • Minimum 5 years clinical research experience plus 2 years leadership in oncology clinical research setting.
  • CITI GCP training required.
  • Knowledge of GCP and US federal clinical research regulations.

Responsibilities

  • Provide proactive leadership and day-to-day oversight to the Clinical Research Coordinator team to support quality patient care and achievement of site-specific performance expectations.
  • Train, coach, and assess staff competency for assigned job responsibilities.
  • Ensure timely and accurate study documentation and communication with monitors and auditors; maintain compliance with GCP and SOPs.
  • Support study acquisition and activation with Shared Services, including protocol review meetings and data collection in Veeva and required systems.
  • Identify and implement practical process improvements that support patients, staff, and site operations.
  • Review incoming protocols for operational feasibility focusing on workload, workflow, and site readiness.
  • Coordinate with Regulatory, Quality, Site Development, Pharmacy, Finance, and other teams to promote compliant study delivery.
  • Support use of CTMS and EHR to ensure accurate documentation and data capture.

Skills

Leadership
Staff coaching
Regulatory knowledge
Communication
Project coordination

Education

Associate’s degree in health administration/nursing/related field
Bachelor’s or Master’s degree (preferred)
Specialty certification in research (preferred)

Tools

CTMS
Veeva
EHR
Microsoft Office

Job description

The START Center for Cancer Research is seeking a Supervisor, Research Coordinator to lead the Clinical Research Coordinator team and ensure study conduct complies with GCP and START standards. You will collaborate with Nursing, Data Coordination, and Shared Services to support clinic operations, study activation, and quality activities.

The role emphasizes staff training, workload planning, and performance oversight in an oncology-focused environment, with regular M-F hours and fixed site

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