Clinical Research Coordinator

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  JOB DUTIES
  

The Semel Institute for Neuroscience and Human Behavior is seeking to hire a full-time Clinical Research Coordinator to join the SUthana Laboratory. You will contribute to the overall operational management of clinical activities from design, set up, conduct, through closeout. Primary duties include: * Coordinating research studies (MRI and TMS) * Facilitating informed consent process * Managing all documentation required by the FDA, CFR, GCP Guidelines, or funding source * Managing all patient registration, data, and treatment assignment * Quality control and quality assurance activities * Completing role-based training and occupational training * Assisting with MRI scanning and TMS treatment of participants * Data collection * Other duties as assigned Salary: $32.65/hr – $52.53/hr

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  JOB QUALIFICATIONS
  

Bachelor’s degree in science related field or Minimum 1 year of experience of previous study coordination or clinical research coordination Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research Matlab and/or Unity programming knowledge (preferred) Working knowledge of the clinical research regulatory framework and institutional requirements Mathematical skills sufficient to prepare clinical research budgets Strong verbal and written communication skills Typing and computer skills including word-processing, use of spreadsheets, email, data entry Analytical skills sufficient to solve and address problems Strong organizational capabilities to organize multiple projects and competing deadlines