Coordinator - Oncology Research - LCI Clinical Trials
Date Posted: Mar 16, 2021
Charlotte, NC, United States
Job ID: 3797
Job Family: Research Services
Status: Full Time
Shift Details: Regular
Department Name: 11011036640304-Clinical Trials - LCI
Location: LCI - 1021 Morehead Medical Dr
Coordinates the clinical, regulatory, business, and other research- related activities and documentation for clinical trials conducted, follows industry standards and applicable regulations including FDA/OHRP guidance, GCP and ICH.
- Fulfills the job responsibilities of the Oncology Research Specialist, and:
- Coordinates clinical and regulatory document submissions for clinical trial start-up, consent development and amendment, protocol amendment, continuing review, closure to accrual, action letter, suspension, termination and other reportable regulatory information.
- Assesses patient eligibility through chart reviews and patient/family interviews.
- Assists in providing patient education regarding the nature of their disease and the benefits/risks of participating in a clinical drug trial.
- Collaborates with regulatory team, Principal Investigator, Sub-Investigators, study personnel, IRB, sponsor/CRO/monitor and other internal/external customers; coordinates documentation/submissions. Conducts routine NCI research base/sponsor website reviews to identify regulatory updates and actions required.
- Presents and obtains patient informed consent.
- Coordinates accurate data collection and record keeping by reviewing documents and processes for quality assurance and ensures timely and accurate submission of data.
- Coordinates and prepares for internal and external audits.
- Participates in sponsor study start-up and follow-up meetings as appropriate.
- Develops study calendars.
- Collaborates on billing and financial activity with Research Finance (budgets and billing compliance).
- Coordinates scheduling of patient visits, labs, and diagnostic procedures.
- Coordinates drug shipments, storage, and accountability with IDS/Pharmacy.
- Assists in the development, improvement and review of Standard Operating Procedures and processes.
- Provides educational and technical assistance to research staff including orientation and mentoring of new research teammates
- Primary owner and serves as a key resource for the Protocol Review Committee Coordinator (PRC)/Investigator-Sponsor Research Committee Coordinator (ISRC)
- Conduct PRC and ISRC training as applicable
- Maintenance of ePRMS console in OnCore
- Document output from PRC and ISRC meetings in OnCore
- Preparation of meeting minutes and ensuring minutes are approved by the PRC and ISRC Chair
- Prepare PRC and ISRC agendas for meetings
- Facilitation of communication with the investigators regarding PRC and ISRC decisions
Primarily works in an office setting. Requires full range of body motion; sitting for extensive periods of time; walking, standing, reading, and writing/keyboarding. Occasionally lifts and carries items weighing up to 35 pounds. Requires corrected vision and hearing within normal range. Must speak and read/write clearly in English. Must be able to be mobile within the entire healthcare system and other locations that participate in LCI clinical trials.
Education, Experience and Certifications
Bachelor's Degree and 1 year of clinical research experience with a pharmaceutical company or Contract Research Organization (CRO) or equivalent experience required; or Master's Degree and 0-1 year of clinical research experience with a pharmaceutical company or Contract Research Organization (CRO) or equivalent experience required; or a minimum of 3 years clinical research experience with a pharmaceutical company or Contract Research Organization (CRO) or equivalent experience required with no degree. Health/Science degree preferred. Previous experience in a healthcare setting preferred, especially cancer care and/or clinical research. Certification in clinical research (SoCRA, ACRP, RAPS, etc.) preferred.