Oncology Clinical Research Coordinator II
Actalent · Palo Alto, CA · 3 wk ago
On-siteResearch$37–$45/hrContract
Qualifications
- Minimum 3.5+ years of Clinical Research Coordinator (CRC) experience
- Oncology clinical research experience required
- Experience supporting Phase I clinical trials, including first-in-human cancer studies
- Experience working within a Bone Marrow Transplant (BMT) program strongly preferred
- Strong clinical research coordination and study management experience
- Proficiency with electronic medical records (Epic preferred)
- Experience with clinical data entry, data management, and regulatory documentation
Responsibilities
- Independently manage significant components of large oncology studies or oversee all aspects of smaller clinical research studies.
- Coordinate and execute Phase I oncology clinical trials, ensuring protocol compliance and participant safety.
- Oversee subject recruitment, screening, enrollment, and retention efforts to meet study goals.
- Develop and manage systems for data collection, organization, monitoring, reporting, and quality control.
- Extract, analyze, interpret, and report study data accurately and efficiently.