Senior Clinical Research Coordinator Oncology, Onsite at Accellacare
Overview
Own oncology clinical trial coordination at multiple sites within the Accellacare network, driving patient recruitment and study execution at scale. Work with a cross functional team to ensure GCP, SOP, and ICH guidelines are followed. Collaborate with managers, monitors, and sponsors to deliver reliable trial outcomes. This role offers visibility across a national network and opportunities for training and business development.
What You'll Do10
- 1Build recruitment plans and tools to generate randomized patients and maximize retention
- 2Design and execute trial logistics including lab work, physiologic testing, and data capture
- 3Lead and mentor CRC Level I and II in trial conduct and protocol requirements
- 4Maintain ongoing communication with monitors and sponsors to report recruitment status and site needs
- 5Travel to Accellacare sites to support trials and participate in site evaluations
- 6Develop relationships with physician investigators and promote the site for future studies
- 7Attend investigator meetings and ensure proper documentation for regulatory compliance
- 8Oversee adverse event reporting and timely notification of investigators and IRB
- 9Assist in training of support staff and other coordinators for protocol adherence
- 10Engage in prospective business development and recruitment of new sites and relationships
Requirements6
- 1Oncology clinical research experience
- 23+ years as a Clinical Research Coordinator
- 3Phlebotomy and clinical skills
- 4Strong understanding of clinical trial processes, GCP, and site documentation
- 5Bachelor’s degree in life sciences, healthcare, or related field
- 6Ability to travel to multiple Accellacare sites as needed
Salary Insight
Salary not disclosed in listing
Location
Required Skills
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