Team Lead - Clinical Research Coordinator

Responsibilities

Cancer Specialists of North Florida is recruiting for an experienced Clinical Research Coordinator Team Lead for our busy Specialty Practice . The Clinical Research Coordinator (CRC) Lead will be responsible for executing key deliverables including the conduct and compliance of clinical trial activities while ensuring quality patient focused care. The CRC Lead will work closely with the research manager to develop new programs and implement new processes for research program improvement. The CRC Lead will be responsible for managing the daily activities of the CRC team and integration of team into clinical sites. Travel is required as the CRC Lead will serve as a back-up CRC and float to sites to provide support as needed. In addition to this, the CRC Lead assists the research team, physicians and manager with any additional projects requested. Essential Duties and Responsibilities include the following:

• Maintain and expand collaborations with pharmaceutical partners, CROs, and other 3 rd parties to grow research portfolio
• Assist research manager with study qualification and study feasibility activities
• Serve as a resource for CRCs and research staff regarding clinical trials, study protocols, and clinical content
• Serve as a back-up CRC and provide on-site coverage as needed
• Assist and oversee training of new CRC hires
• Supervise CRC team in conduct of clinical trial activities including but not limited to recruitment, screening, enrollment, scheduling, dosing, adverse event monitoring, vital collection, and IVRS management
• Serve as a resource and educator for CRCs and staff regarding clinical trials and study protocols
• Answer escalated study-specific inquiries that requires clinical expertise/knowledge and ability to apply said knowledge to clinical trial
• Collaborate with research manager and team on continuous process improvement and quality assurance (QA) projects to assure consistent standard of practice and patient care provided
• Oversee accurate data collection, documentation, and timely query resolution
• Collaborate with regulatory team to maintain on-site equipment calibration and training
• Monitor CRC compliance with study protocol and study-related activities
• All other duties as assigned
  
  

Full-time position

Education And Experience

• Bachelor’s degree in science or health related field; BSN, PharmD, MD, or PhD preferred
• 2 years of experience in working with complex clinical trials from a site, sponsor, or CRO perspective with a preferred focus on oncology and/or hematology
• 2 years management experience
• Data Quality Assurance (QA)/auditing experience is a plus
  
  

Certificates, Licenses, Registrations

• CCRP, preferred
  
  

Compensation And Benefits

• Salary is commensurate with experience and qualifications
  
  

Cancer Specialists of North Florida is an "EEO Employer” and “Drug Free Workplace”