UNIV - Program Coordinator - Psychiatry: Brain Stimulation Laboratory

Medical University of South Carolina•Charleston, SC

About The Position

The Department of Psychiatry & Behavioral Sciences 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.

Requirements

A bachelor's degree and two years of relevant program experience.

Nice To Haves

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 participant comfort during procedures and for being sensitive to any potential distress.

Responsibilities

Manage, oversee, and train a team of research coordinators across multiple studies in the lab.
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.
Participate in feasibility and logistical planning for new and ongoing studies.
Serve as an expert in acquisition and execution of studies using MRI, EEG, TMS, eyetracking, fNIRS, behavioral, diagnostic, physiological, and other complex data types.
Coordinate data management collection according to the protocol requirements and compliance.
Create and maintain accurate and comprehensive records as required by the FDA, the IRB, study sponsors and Good Clinical Practice Guidelines.
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.
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.
Design and build RedCap databases as necessary for investigator-initiated studies.
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.