Research Coordinator CMC
Carolinas Healthcare
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Post Date: Nov 15, 2017
Job Type: Full time
Start Date: - n/a -
Salary: - n/a -
Location: US - North Carolina - Charlotte
Job Reference: 146271-en_US
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Description
Job Req ID: 146271Position Number: 00157552Employment Type: Full TimeShift: Variable/On CallShift Details: 8:00am-4:30pmStandard Hours: 40.00Department Name: OPR Oral MedicineLocation: Therapeutic Research and DevelLocation Details:  CMC   Job Summary
Manages protocols to ensure the safety of patients and quality of clinical trial data. Prepares and submits Institutional Review Board (IRB) paperwork and maintains all related regulatory document submissions.

Essential Functions
    Assists in providing patient education regarding the nature of their disease and the benefits and risks of participating in a clinical drug trial.Determines protocol-related needs to conduct the trial and orders supplies and equipment.Recruits and screens potential patients and obtains informed consent.Assists in providing patient education and benefits and risks of participating in a clinical drug trial.Designs organizational tools and forms to facilitate accurate data collection and recordkeeping.Conducts in-service programs, summarizes study schedule to assist in understanding and implementing a protocol.Manages research funds.Schedules patient visits and laboratory and diagnostic test procedures.Coordinates drug shipments, storage, and accountability with pharmacy.Reviews trends, problems encountered, patient adverse events, and patient progress.Conducts clinical research encounters/participant visits following protocol requirements, to include biological sample collection.
 Physical Requirements
Works in clinical care areas and office environments. May be required to travel. Requires close, personal contact with patients, handling of blood and body fluids, walking, sitting, standing, lifting, handling of charts, supplies and equipment, and operation of a keyboard and computer. Responsibility to work in a safe manner.

Education, Experience and Certifications
Bachelors Degree and research experience required. Masters Degree preferred. Understanding of the human subject research regulatory requirements (Good Clinical Practices (GCP), International Conference on Harmonization (ICH) Guidelines, as well as applicable rules/regulations pertaining to research; knowledge of regulatory requirements of the Food and Drug Administration (FDA), Institutional Review  Boards (IRB), and Human Subjects Protections (OHRP) pertaining to clinical research). Phlebotomy experience.
   At Carolinas HealthCare System, our patients, communities and teammates are at the center of everything we do. Our commitment to diversity and inclusion allows us to deliver care that is superior in quality and compassion across our network of more than 900 care locations. As a leading, innovative health system, we promote an environment where differences are valued and integrated into our workforce. Our culture of inclusion and cultural competence allows us to achieve our goals and deliver the best possible experience to patients and the communities we serve. Posting Notes: Not ApplicableCarolinas HealthCare System is an EOE/AA Employer



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