Clinical Research Coordinator at START Center for Cancer Research
Overview
Join the START Center for Cancer Research as a Clinical Research Coordinator. You will lead daily activities of early phase oncology clinical trials while supporting senior research staff. This role ensures accurate and timely conduct of clinical research following protocols and regulatory standards.
What You'll Do12
- 1Communicate regularly with Study Sponsors CROs and staff regarding protocol questions and status updates
- 2Monitor day-to-day conduct of assigned studies according to SOPs and Good Clinical Practice guidelines
- 3Create and review trial forms to ensure protocol compliance
- 4Maintain standardized study document labeling and filing procedures
- 5Implement initial protocol and amendments while training staff involved in patient treatment
- 6Keep an up-to-date contact list and assist with patient screening and eligibility determination
- 7Facilitate informed consent processes and prepare source documents per SOPs
- 8Identify protocol deviations and collaborate with leadership to resolve corrective actions
- 9Assist data coordination team with case report form completion and query resolution
- 10Work with Principal Investigators on Serious Adverse Event reporting and closeout activities
- 11Provide patient education on trial participation and medication side effects
- 12Perform telephone triage assessments when required
Requirements8
- 1High School Diploma or GED
- 22 years of clinical research experience
- 3Basic understanding of oncology clinical trials especially Phase 1 studies
- 4Strong attention to detail and accuracy in data collection
- 5Proficiency in Microsoft Office Suite and clinical trial management software
- 6Experience in oncology settings preferred
- 7Fast-paced environment with demanding deadlines
- 8Commitment to continuous learning and knowledge updates
Salary Insight
Salary not disclosed in listing
Location
Required Skills
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