Clinical Research Coordinator

START Center for Cancer Research-posted 2 days ago
Full-time • Entry Level
West Valley City, UT
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Join the world's largest early phase oncology clinical research network! The START Center for Cancer Research is revolutionizing cancer treatment through groundbreaking clinical trials that bring hope directly to patients. With an impressive global footprint spanning the United States, Spain, Portugal, and Ireland, we've completed over 1,300 studies that have led to 45 FDA/EMA approved therapies—including being the first to treat a patient with Keytruda, the most effective cancer drug in medical history. Unlike traditional Academic Medical Centers that reach only 20% of cancer patients, START brings cutting-edge trials directly to community hospitals where most patients receive care. By joining our team, you'll be part of an organization that's truly changing lives and shaping the future of cancer treatment worldwide. Learn more at STARTresearch.com . We are hiring a Clinical Research Coordinator for our West Valley City, UT location. The Clinical Research Coordinator (CRC) supports early-phase oncology trials under senior research staff guidance. Ensuring compliance with protocols, regulations, and patient safety standards, the CRC manages patient participation, data collection, and adherence to Good Clinical Practice (GCP). Overseeing multiple protocols, they coordinate trial activities, implement protocol requirements, and provide accurate updates to the research team. Schedule : Monday through Friday, 8am-5pm

  • Communicate regularly with study sponsors, CROs, and staff regarding protocol status, questions, and concerns.
  • Monitor daily study conduct to ensure compliance with protocols, SOPs, and Good Clinical Practice.
  • Create and review trial forms to maintain protocol compliance.
  • Implement protocols and amendments, training staff involved in patient treatment and management.
  • Assist with patient screening, eligibility determination, and the informed consent process.
  • Identify and address protocol deviations, coordinating corrective actions with leadership.
  • Support data coordination, including case report form completion, query resolution, and closeout activities.
  • High School Diploma or GED.
  • 2 years of clinical research experience.
  • Basic understanding of oncology clinical trials, particularly Phase 1 studies.
  • Strong attention to detail and accuracy in data collection and documentation.
  • Ability to manage multiple tasks and meet deadlines in a fast-paced environment.
  • Excellent organizational and time-management skills.
  • Strong communication skills, both written and verbal.
  • Ability to interact professionally with patients, study staff, and external stakeholders.
  • Working knowledge of GCP and regulatory requirements.
  • Proficient in Microsoft Office Suite and clinical trial management software.
  • Experience working in an oncology setting.
  • Comprehensive health coverage: Medical, dental, and vision insurance provided
  • Robust retirement planning: 401(k) plan available with employer matching
  • Financial security: Life and disability insurance for added protection
  • Performance recognition: Annual 10% bonus opportunity based on performance
  • Career development: Educational assistance program to support your professional growth
  • Financial flexibility: Health savings and flexible spending accounts offered
  • Well-being and work-life balance: Generous paid time off and paid holidays, flexible schedule.
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