ApplyTIME Clinical Research Coordinator
Posted about 2 months agoViewed
View full description
💎 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.
Apply