Clinical Research Coordinator

Location
Norfolk, VA
Salary
Competitive
Posted
Oct 29, 2020
Closes
Dec 07, 2020
Ref
140268BR
Function
Other
Industry
Healthcare
Hours
Full Time
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 as 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. As the primary resource for the protocols, will act as liaison between the investigators, the institutional review board (IRB), and the sponsor.

Qualifications

Education Level
Bachelor's Level Degree - Experience in lieu of education: Yes

Experience
Required: Clinical - 2 years, Research - 2 years

Preferred: None, unless noted in the "Other" section below

License
Required: Basic Life Support

Preferred: None, unless noted in the "Other" section below

Skills
Required: Active Listening, Communication, Coordination, Critical Thinking, Mathematics, Mgmt of Financial Resources, Microsoft Excel, Microsoft PowerPoint, Microsoft Word, Monitoring, Project Management, Reading Comprehension, Science, Service Orientation, Social Perceptiveness, Speaking, Time Management, Writing

Preferred: None, unless noted in the "Other" section below

Other
2 years Clinical or Research experience required with Bachelor's degree. In lieu of BS, 1) certified clinical professional (CMA/RMA, RN, LPN or MLT as applicable) with 5 years of clinical experience or 2) 5 years of clinical research experience (no certifications required). Specialty Certification CCRP, ACRP-CP or CCRC required within 3 years of employment, BLS required within 90 days.

Similar jobs

More searches like this