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UNIV - Program Coordinator - Psychiatry: Brain Stimulation Laboratory

Job in Charleston, Penobscot County, Maine, 04422, USA
Listing for: SupportFinity™
Full Time position
Listed on 2026-01-22
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research, Research Scientist
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Location: Charleston

UNIV - Program Coordinator - Psychiatry:
Brain Stimulation Laboratory

MUSC Health | Posted Jan 16, 2026

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Full-time

Charleston

Entry (0-2 yrs)

Job Description Summary

The Department of Psychiatry & Behaviorals Scienc es is hiring a Program Coordinator II. This position is assigned to the Brain Stimulation Laboratory for the purpose of managing, coordinating, planning and implementing research protocols throughout the lab across multiple studies. The individual will function as an expert and manage a team of researchers in their day-to-day operations, which may include recruitment, testing, sample selections, data recording, and operation of complex non-invasive brain stimulation protocols including Magnetic Resonance Imaging (MRI), Electroencephalography (EEG), Transcranial Magnetic Stimulation (TMS), eye tracking, and functional Near-Infrared Spectroscopy (fNIRS) in human populations including PTSD, addiction, stroke, dementia, depression, and suicide risk.

The Program Coordinator II will oversee regulatory paperwork and communications with the IRB, sponsors, and all other applicable governing bodies. This job will also include career development mentoring and opportunities for those interested in pursuing a career in medicine, neuroscience, psychology or related fields.

Entity

Medical University of South Carolina (MUSC - Univ)

Worker Type

Employee

Worker Sub-Type

Research Grant

Cost Center

CC001044 COM PSYCH Brain Stimulation Medicine CC

Pay Rate Type

Salary

Pay Grade

University-06

Pay Range

47,588.

- 88,047.000

Scheduled Weekly Hours

40

Work Schedule

Monday - Friday, 8:00 am - 5:00 pm

FLSA

Salaried

Job Duties
  • 30%:
    This individual will manage, oversee, and train a team of research coordinators across multiple studies in the lab. They will maintain up-to-date knowledge of relevant studies and perform research activities, including scheduling complex, multi-step study procedures, coordinating with multiple departments, physicians, and study sponsors. They will participate in feasibility and logistical planning for new and ongoing studies.
  • 30%:
    This individual will serve as an expert in acquisition and execution of studies using MRI, EEG, TMS, eye tracking, fNIRS, behavioral, diagnostic, physiological, and other complex data types. They will coordinate data management collection according to the protocol requirements and compliance.
  • 20%:
    This individual will create and maintain accurate and comprehensive records as required by the FDA, the IRB, study sponsors and Good Clinical Practice Guidelines. They will coordinate/ perform the reporting and communications with the IRB and the study sponsor remotely and during monitoring visits as relevant to research protocols, study implementation, adverse events (AEs), ongoing study updates, and other activities necessary for exceptional performance from study activation to close-out.
  • 15%:
    This individual will write Informed Consent Forms (ICFs) and complete IRB-related study maintenance; collaborate with MUSC PIs in protocol writing and study design for investigator-initiated studies; and design and build Red Cap databases as necessary for investigator-initiated studies.
  • 5%:
    This individual will participate in MUSC IRB, VA R&D, and /or Sponsor initiated audits;
    Independently manage Study-specific data and identify data discrepancies and develop corrective action plans; assist with preparation for Data Safety Monitoring Board meetings.
Preferred Experience and Skills

A Master’s degree in Psychology, Neuroscience, Exercise Science, or a related health sciences field. At least 3 years of prior experience working in a research environment is mandatory. At least 3 years of prior experience administering clinical questionnaires and neuropsychiatric cognitive assessments is mandatory. Specifically, at least 1 year of prior experience with EEG, fMRI, FNIRS, Eye tracking, and TMS is mandatory.

1 year experience working with combined fMRI-EEG-TMS and closed-loop EEG-rTMS multimodality systems is required. The ability to use Microsoft office and data processing programs including but not limited to MATLAB, R, and SPSS are very helpful. Strong interpersonal skills are key for promoting…

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