UNIV - Program Coordinator I - Psychiatry: Addiction Sciences Division
Job
MUSC
Charleston, SC (In Person)
$66,549 Salary, Full-Time
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Job Description
UNIV
- Program Coordinator I
Psychiatry:
Addiction Sciences Division 3.6 3.6 out of 5 stars Charleston, SC $45,300- $77,000 a year
- Full-time
MUSC 908
reviews $45,300- $77,000 a year
- Full-time
R-0000061478
Charleston, South Carolina Laboratory Clinical & Research Support Services Full Time University (UNIV) Job Description Summary The candidate will provide technical and professional research services in the Addiction Sciences Division of MUSC. This candidate will support the Principal Investigator in the coordination and execution of research projects/clinical trials. The candidate will work on research studies which focus on the study of and development of interventions for substance use and trauma-related outcomes. The program coordinator will be directly involved in the collection of questionnaires, interview, laboratory, and other research data. Entity Medical University of South Carolina (MUSC- Univ) Worker Type Employee Worker Sub-Type Research Grant Cost Center
CC001039 COM PSYCH
Addiction Science CC Pay Rate Type Hourly Pay Grade University-GEN08 Pay Range 45,300.00- 61,100.00
- 77,000.
Work Shift Job Description FLSA:
Hourly Work Schedule:
Monday- Friday, 8:30 am
- 5:00 pm, with flexibility to cover evening and weekend research appointments
Job Duties:
20%- Manage and/or oversee the day-to-day running of research protocols. Review workload and operating procedures, determine priorities and allocate resources to meet workload requirements. 20%
- Performs diagnostic interviews consisting of structured clinical interviews and other related instruments and document participant assessment data in research records. 15%
- Manage data collection and entry functions, either directly or indirectly through supervision of a research assistant and/or data entry personnel. Coordinate and manage tracking of all research participants. Prepare reports as needed and present status to the research team at weekly meetings. 15%
- Evaluate participants for entry into research study. Assist with screening and recruitment of research participants and coordination of research activities. Document participant assessment data in research records. Collect psychophysiological and biological data through human laboratory methods. 15%
- Complete regulatory documentation for submissions as required. Initiates and maintains accurate and comprehensive documentation as required by the FDA, DOD, Institutional Review Board, study sponsors, and Good Practice Guidelines in connection with research trials. 10%
- Monitors study documentation for compliance with protocols, SOP's, federal, state and local regulations and for safety and effectiveness of research protocol. 5%
- Performs other duties as assigned.
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.
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