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MUSC
UNIV - Regulatory Coordinator - Department of Medicine: Division of Pulmonary
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What they do
A Clinical Research Coordinator directs clinical research and development projects for companies, and coordinates testing and quality control.
$111,127 / year median in South Carolina
+17% projected growth
Job Description
UNIV
- Regulatory Coordinator
Department of Medicine:
Division of Pulmonary MUSC- 3.6 Charleston, SC Job Details Full-time $45,300
- $77,000 a year 1 day ago Qualifications Bachelor's degree Full Job Description
R-0000065295
Charleston, South Carolina Laboratory Clinical & Research Support Services Full Time University (UNIV) Job Description Summary This position will serve as the Regulatory Coordinator for the Clinical Trial Research Program specializing in Pulmonary, Critical Care, Gastroenterology, Endocrinology Nephrology and Hepatology. This position will work with the Program's Clinical Research Coordinators and Clinical Research Program Manager to ensure all deadlines are met. Responsibilities include coordinating and performing study specific regulatory processes for the Program while ensuring that appropriate regulations and Standard Operating Procedures (SOPs) are followed. Entity Medical University of South Carolina (MUSC- Univ) Worker Type Employee Worker Sub-Type Research Grant Cost Center
CC000974 COM DOM PULM
General CC Pay Rate Type Hourly Pay Grade University-GEN08 Pay Range 45,300.00- 61,100.00
- 77,000.
Job Description Job Duties:
25%•Study Start-up and Maintenance:
Receive start-up packet from sponsor; initiate and monitor study start-up activities, including all necessary documents. Upon activation, submit amendments and any changes to the study to the IRB and notify study team of all approvals. Submit continuing reviews. Answer questions and provide documents as requested by the Investigator, Program Manager, and study sponsor. Maintains accurate study registration as applicable (ClinicalTrials.gov, etc) for all investigator-initiated projects; provides guidance on issues such as when to re-consent subjects, when to report events per IRB policy. 20%•Regulatory Documentation:
Maintain all necessary regulatory documents, such as CVs, medical licensure, note-to-files, conflict of interest, laboratory certifications, and any other documents required for the Program's regulatory files. Will be responsible for building electronic regulatory binders and maintaining the electronic files. Oversee regulatory documentation for multi-site projects, with MUSC acting as the lead site; responsible for creating the templates that will be utilized. 20%•Source Documentation:
Create and maintain eSource documentation database for use by research coordinators. Will be responsible for maintaining database for the life of the study from creation to closure. This includes coding and building of source structure, field editing based on protocol amendments or usage needs, creating reports and alerts as needed, and alerting study team of any changes made. 15%- Study monitoring and audit visits: Ensure all documents are complete and filed (either physically or electronically) in the regulatory binder.
Administrative:
Will provide administrative support as needed to the Program Manager, Accountant Fiscal Manager, Education & Operations Specialist, Accountant/Fiscal Analyst, and Regulatory Manager. Examples include, scheduling meetings, providing assistance to any Program events, completing site tours, and other tasks as needed. 5%Safety Reporting:
Completes IRB and/or sponsor reportable events independently. Applies protocol and institutional guidelines to differentiate between reportable vs. non-reportable adverse events. 5%
Other:
Assist with other study tasks or projects as needed.Additional Job Description Minimum Requirements:
A bachelor's degree and one year of relevant program experience.Physical Requirements:
(Note:
The following descriptions are applicable to this section: Continuous- 6-8 hours per shift; Frequent
- 2-6 hours per shift; Infrequent
- 0-2 hours per shift) Ability to perform job functions in an upright position.