Clinical Research Coordinator - Float

Cancer Specialists LLC•Jacksonville, FL

13d

About The Position

Cancer Specialists of North Florida is recruiting a Clinical Research Coordinator - Float for our busy Specialty Practice. The Clinical Research Coordinator (CRC) Float will facilitate timely coordination of daily clinical trial activities across multiple research projects and ensure trial protocol compliance. The CRC is responsible for recruitment, screening, consenting, enrollment, and clinical documentation of patients in clinical trials as well as ensuring protocol compliance. The CRC will provide education to patients and staff about trial concepts and requirements for participation. The CRC will work collaboratively with the clinical site, sponsor(s), clinical research organization(s) (CROs), institutional review boards (IRBs), and study participants to ensure execution of the clinical trial in accordance with the trial protocol, Food and Drug Administration (FDA), Good Clinical Practice (GCP) guidelines, and applicable state and local regulations. In addition to this, the CRC assists the research team, physicians and manager with any additional projects requested. Essential duties and responsibilities include the following:

Requirements

Bachelor’s degree in science or health related field
2+ years of work as a clinical research coordinator in an oncology setting

Nice To Haves

BSN, PharmD, MD, or PhD preferred

Responsibilities

Review and develop a familiarity with trial protocol including but not limited to study proceedings and timelines, inclusion and exclusion criteria, confidentiality, and privacy protection
Serve as a resource and “expert” for clinical staff and patients regarding clinical trial questions
Ensure compliance with research protocols by providing ongoing quality control audits
Provides CRC coverage to all CSNF clinics as assigned by manager or team lead.
Strong interpersonal and communication skills to effectively collaborate with clinic site staff and research staff.
Recruit and screen potential study participants and perform intake assessments for assigned clinical trials in accordance with trial protocol
Obtain informed consent in accordance to the Code of Federal Regulations (45 CFR part 46)
Coordinate all study visits and assist treating physician with completion of trial activities including but not limited to: schedule participant visits, coordinate participant travel and meals, participant dosing and observation, scheduling and other evaluations, adverse event monitoring, vitals collection, and IVRS management
Collect, process, and ship specimens
Collaborate with the research pharmacist to perform drug accountability, compliance, and dosing
Educate clinical staff regarding study drug administration requirements, including required pre-medications, order of administration, monitoring time points, and the need for infusion start/stop times
All other duties as assigned.