Description

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/hrQualifications

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

UCLA Health welcomes all individuals, without regard to race, sex, sexual orientation, gender identity, religion, national origin or disabilities, and we proudly look to each person’s unique achievements and experiences to further set us apart.