Clinical Research Coordinator - Neurology (part-time)

Description

The Stroke Center within the Department of Neurology is seeking a Clinical Research Coordinator to support its clinical research projects. The coordinator will play a central role in the operational management of clinical studies, overseeing activities from study setup through conduct and closeout. In this role, you will be responsible for implementing research activities for one or more studies, managing projects, and prioritizing work to meet deadlines. You will plan and organize tasks to ensure adherence to study protocols and compliance with institutional policies, FDA regulations, and ICH Good Clinical Practice guidelines. The coordinator will collaborate with the Principal Investigator, ancillary departments, sponsors, and other institutions to support all aspects of study administration, including regulatory compliance, and overall project support.

Hourly salary range: $38.19 - $61.45. The department’s target salary is $38.19.

Qualifications

Required:

Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience

Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.

Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness.

Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment.

Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.

Ability to respond to situations in an appropriate and professional manner.

Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.

Ability to be flexible in handling work delegated by more than one individual.

Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications.

Ability to handle confidential material information with judgement and discretion.

Working knowledge of the clinical research regulatory framework and institutional requirements.

Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.

Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.

Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc.

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