JOB DUTIES
Description
Join as a Clinical Research Coordinator, managing pivotal phases of clinical research activities from design to closeout. Responsibilities include implementing research activities, ensuring adherence to protocols, and prioritizing tasks to meet deadlines. Collaborate with stakeholders, PI, departments, and sponsors to oversee compliant conduct and support study administration. Salary: $32.65 – $52.53/hour
JOB QUALIFICATIONS
Qualifications
Required: * 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. Preferred: * Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience * 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. * Fluent in writing and speaking Spanish.
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