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Clinical Research Coordinator I

Job ID: 14273
Facility:
City: Greensboro

Date Posted: 2020-07-30 06:11:59 UTC
2020-07-30 06:11:59 UTC

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Job Description

LOCATION:LeBauer Pulmonary Care, LB-Pulmonix Research
CITY: Greensboro, NC

JOB DETAILS:
Exempt: No | FTE: 1.0 (40 hours/week) | Schedule: Monday - Friday, 7:45 AM - 4:45 PM | On Call: YES

JOB SUMMARY:
Clinical Research Coordinator (CRC) I is an entry level professional title in the Clinical Research Coordinator Family. CRC I's, work closely with study subjects and other research staff, and are involved in most steps of the research trial process. CRC's participate in clinical research studies conducted by principal investigator(s) including, but not limited to, grant funded research and/or industry sponsored clinical research conducted on site at Cone Health or its affiliated sites; performs a variety of duties involved in the collection, compilation, documentation and analysis of clinical research data. They function under the Principal Investigator's medical license and cannot perform any tasks that by state or local law require a license to perform. Their work is routine in nature, with assignments provided at a task level, focused on the long term goals of clinical research trial and process. CRC I's have no supervisory responsibilities and work under immediate supervision.

EDUCATION:

Required: Associate's degree and four years of relevant experience. Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification, along with a minimum of two years additional professional experience, will be considered in place of degree. Any degree substitutions are subject to review by committee.

Preferred: Bachelor's degree and one year of clinical research experience.

EXPERIENCE:
Preferred: List preferred length and type of experience.

LICENSURE/CERTIFICATION/REGISTRY/LISTING:

REQUIRED
Required:
1. Understanding of ICH/GCP guidelines for human research.
2. Understanding of Code of Federal Regulations for Human Subjects.
3. Computer Competency including proficiency in Microsoft Office and EDC systems.
4. Understanding Phases I-IV drug development processes.
5. Technical skills related to the completion of a study visit as required by the protocol.

Obtain Good Clinical Practice certification within 30 days of hire and maintain without lapse.

Obtain Human Subjects Research certification within 30 days of hire and maintain without lapse.

PREFERRED
Preferred: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is preferred. Required if candidate does not have Bachelor's degree

Cone Health is an equal opportunity employer. If you require assistance with our online job submission process, please contact our team at 866-266-3767 to request an accommodation.
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