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TIME Clinical Research Coordinator

Posted about 2 months agoViewed

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💎 Seniority level: Junior, 2+ years

📍 Location: Unincorporated Los Angeles

🔍 Industry: Healthcare and clinical research

🏢 Company: Tempus👥 1001-5000💰 $100,000,000 Debt Financing about 2 years agoArtificial Intelligence (AI)BiotechnologyMedicalMachine LearningPrecision MedicineHealth Care

🗣️ Languages: English

⏳ Experience: 2+ years

🪄 Skills: Project ManagementProject CoordinationCommunication SkillsAnalytical SkillsCollaborationMicrosoft ExcelProblem SolvingMicrosoft OfficeAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communicationMultitaskingDocumentationMicrosoft Office SuiteMS Office

Requirements:
  • Candidate must have a Bachelor’s degree in Life Sciences or a health-related field.
  • 2+ years of clinical research experience in an oncology setting.
  • Knowledge of current FDA regulations, Good Clinical Practices (GCP's), and HIPAA.
  • CCRC preferable.
  • Strong planning and project management skills.
  • Excellent organization and communication skills with high attention to detail.
  • Proficiency with EDC systems and database management.
  • Proficiency with MS Office applications (Word, Excel, PowerPoint).
Responsibilities:
  • Educate and provide status updates to physicians and research staff regarding clinical trials in the TIME program portfolio.
  • Oversee the Tempus generated patient matches and maintain the patient tracker.
  • Screen potential study participants for available TIME trials.
  • Prepare rapid study activations for just-in-TIME trials and assist as needed during start-up.
  • Ensure all clinical trial data is entered into electronic data capture (EDC) systems efficiently.
  • Participate in research meetings and ensure startup timelines are met.
  • Create site support tools and TIME trial related communications.
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