Sentara Healthcare Inc
Clinical Research Coordinator- Virginia Beach, VA
Sentara Healthcare Inc, Virginia Beach, Virginia, us, 23450
Overview
Sentara Health is hiring a Clinical Research Coordinator for the Clinical Trials office. This is a TEMPORARY Full-time, Day shift position. Working hours are 8:00 am to 4:30 pm. Local travel throughout Hampton Roads is required on a daily basis. The project is estimated to continue for approximately 18-24 months. Responsibilities
Manages and coordinates all aspects of conducting clinical trials within Sentara Health, both clinically and administratively. Utilizes in-depth knowledge of protocol requirements to ensure that studies are properly conducted in conformance with the protocol guidelines, departmental standards and good clinical practices as set forth by federal regulations. Responsible for the sound conduct of the clinical trial including recruitment, screening, enrollment and follow-up of eligible subjects according to protocol requirements. Maintains accurate and complete documentation of related regulatory documents. Serves as the primary resource for the protocols and acts as liaison between the investigators, the institutional review board (IRB), and the sponsor. Education
Bachelors Degree preferred. Certification/Licensure
Basic Life Support (BLS) - Certification - American Heart Association (AHA) RQI required within 90 days. Certified Clinical Research Professional (CCRP), Association of Clinical Research Professionals - Certified Professional (ACRP-CP) or Certified Clinical Research Professional (ACRP-CCRC) required within 3 years of employment. Experience
Three years Clinical Research experience preferred. Epic EMR experience preferred. Phlebotomy experience preferred. Keywords: Talroo-Health Plan, Talroo-Nursing, LinkedIn, CCRP, ACRP-CP, ACRP-CCRC, clinical trials, research, oncology, cancer screening, grant, national cancer institute.
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Sentara Health is hiring a Clinical Research Coordinator for the Clinical Trials office. This is a TEMPORARY Full-time, Day shift position. Working hours are 8:00 am to 4:30 pm. Local travel throughout Hampton Roads is required on a daily basis. The project is estimated to continue for approximately 18-24 months. Responsibilities
Manages and coordinates all aspects of conducting clinical trials within Sentara Health, both clinically and administratively. Utilizes in-depth knowledge of protocol requirements to ensure that studies are properly conducted in conformance with the protocol guidelines, departmental standards and good clinical practices as set forth by federal regulations. Responsible for the sound conduct of the clinical trial including recruitment, screening, enrollment and follow-up of eligible subjects according to protocol requirements. Maintains accurate and complete documentation of related regulatory documents. Serves as the primary resource for the protocols and acts as liaison between the investigators, the institutional review board (IRB), and the sponsor. Education
Bachelors Degree preferred. Certification/Licensure
Basic Life Support (BLS) - Certification - American Heart Association (AHA) RQI required within 90 days. Certified Clinical Research Professional (CCRP), Association of Clinical Research Professionals - Certified Professional (ACRP-CP) or Certified Clinical Research Professional (ACRP-CCRC) required within 3 years of employment. Experience
Three years Clinical Research experience preferred. Epic EMR experience preferred. Phlebotomy experience preferred. Keywords: Talroo-Health Plan, Talroo-Nursing, LinkedIn, CCRP, ACRP-CP, ACRP-CCRC, clinical trials, research, oncology, cancer screening, grant, national cancer institute.
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