Clinical Research Coordinator
: Job Details :

City/StateCharlottesville, VAOverviewWork ShiftFirst (Days) (United States of America)Sentara Martha Jefferson Hospital is now hiring a full-time, Clinical Research Coordinator. Job duties/Responsibilities:Manages and coordinates all aspects of conducting clinical trials within Sentara Healthcare, 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 set forth by federal regulations. Sound conduct of the clinical trial including recruitment, screening, enrollment and follow-up of eligible subjects according to protocol requirements. Maintenance of accurate and complete documentation of related regulatory documents. Participates in writing, presenting, and publishing results of studies. As the primary resource for the protocols, will act as liaison between the Investigators, the institutional review board (IRB), and the Sponsor.RequirementsBachelor's degreePrior work experience with clinical trials. Knowledge of patient consenting process along with regulations around clinical trials is highly preferred.Benefits

• Medical, Dental, Vision insurance
• Paid Time Off
• Tuition Reimbursement
• 401k/403B with matching funds,
• Retirement Pension
• Performance Plus Bonus
• Career Advancement Opportunities
• Work Perks, and more.

Visit to view what great benefits we have to offer!#indeed, clinical research, clinical trialsJob SummaryManages and coordinates all aspects of conducting clinical trials within Sentara Healthcare, 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 set forth by federal regulations. Sound conduct of the clinical trial including recruitment, screening, enrollment and follow-up of eligible subjects according to protocol requirements. Maintenance of accurate and complete documentation of related regulatory documents. Participates in writing, presenting, and publishing results of studies. As the primary resource for the protocols, will act as liaison between the Investigators, the institutional review board (IRB), and the Sponsor.BSN required. Specialty certification Certified Clinical Research Professional (SOCRA CCRP or ACRP-CP) or Certified Clinical Research Coordinator (CCRC) is required within 3 years of employment. 2 years of research OR nursing experience required. BLS required within 90 daysQualifications:N-4YR - RN-Bachelor's Level Degree (Required)Basic Life Support (BLS) - Certification - American Heart Association (AHA) RQI, Registered Nurse (RN) Single State - Nursing License - North Carolina, Registered Nurse (RN) Single State - Nursing License - Virginia Department of Health Professionals (VADHP), Registered Nurse License (RN) - Nursing License - Compact/Multi-State LicenseClinical, ResearchSkillsActive Listening, Communication, Coordination, Critical Thinking, Mathematics, Mgmt of Financial Resources, Microsoft Excel, Microsoft Office, Microsoft PowerPoint, Microsoft Word, Monitoring, Project Management, Reading Comprehension, Science, Service Orientation, Social Perceptiveness, Speaking, Time Management, WritingSentara Healthcare prides itself on the diversity and inclusiveness of its close to an almost 30,000-member workforce. Diversity, inclusion, and belonging is a guiding principle of the organization to ensure its workforce reflects the communities it serves.Per Clinical Laboratory Improvement Amendments (CLIA), some clinical environments require proof of education; these regulations are posted at ecfr.gov for further information. In an effort to expedite this verification requirement, we encourage you to upload your diploma or transcript at time of application.In support of our mission to improve health every day, this is a tobacco-free environment.