CLINICAL TRIALS RESEARCH COORD - (greenville, south carolina) in Greenville, South Carolina For Sale
Job Class 13;
CLINICAL PROFESSIONAL 13;
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FLSA 13;
Exempt 13;
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Job Summary 13;
Responsible for the implementation, management and oversight of clinical trial research studies including the education of research staff, healthcare team member, participants and their caregivers. Registers, compiles, submits and oversees clinical data, monitors study compliance and maintains a system for effective data flow for patients on clinical trials. Manages patient visits and implements protocol related procedures. Responsible for monitoring and communicating study participant progress and safety issues with the investigators, applicable regulatory agencies, health care team and study staff.
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Supervisory/Management Responsibilities 13;
This is a non:management job that will report to a supervisor, manager, director or executive. 13;
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Minimum Education 13;
Other : Associate degree in Allied Health OR Bachelors Degree in health sciences or business.
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Minimum Experience 13;
1 Year : Research experience in at least one of the following areas: pharmaceutical, academic, device, NIH, investigator initiated studies or registry trials.
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Required Certifications/Registrations/Licenses 13;
JOB RELATED CERTIFICATION : COTR 13;
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Specific Acceptable Credentials (if applicable) 13;
If Allied Health Degree: South Carolina certification/license in field.
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In lieu of the Above Minimum Requirements 13;
The following requirements will also be considered in lieu of 1 year research experience:
Associate Degree in Allied Health plus 3 years direct experience in that field
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Bachelor Degree in a science and 3 years direct experience in that field.
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Other Required Experience 13;
International Air Transport Association Certification : Preferred
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Position Posting Category 13;
Clinical Professional/Technical
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