UNIV - Program Coordinator I - Psychiatry: Addiction Sciences Division
Listed on 2026-08-17
-
Research/Development
Clinical Research, Research Assistant/Associate, Research Scientist, Research Analyst
UNIV
- Program Coordinator I
- Psychiatry:
Addiction Sciences Division
Charleston, South Carolina
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.
Medical University of South Carolina (MUSC
- Univ)
Employee
Research Grant
CC001039 COM PSYCH Addiction Science CC
Hourly
University-GEN
08
45,300.
- 77,000.000
40
Monday
- Friday, 8:30 am - 5:00 pm, with flexibility to cover evening and weekend research appointments
Job Duties:
- 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.
- Performs diagnostic interviews consisting of structured clinical interviews and other related instruments and document participant assessment data in research records.
- 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.
- 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 psycho-physiological and biological data through human laboratory methods.
- 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.
- Monitors study documentation for compliance with protocols, SOP's, federal, state and local regulations and for safety and effectiveness of research protocol.
- Performs other duties as assigned.
Minimum Requirements:
A bachelor's degree and one year of relevant program experience.
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