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of technology, innovation and discovery improving patient outcomes. The Clinical Research Associate II works independently but in close collaboration with a Clinical Research Coordinator, Research Program
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supporting the informed consent process. Responsible for accurate and timely data collection, documentation, entry and reporting, including resolution of queries from sponsors or regulatory entities
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. The Associate will observe and comply with safety standards and procedures, assist in preparation of data for publication and/or presentation at scholarly meetings, and assist in general laboratory maintenance
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tasks supporting the coordination/implementation of noncomplex research studies. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential and
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concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response
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. Performs other assignments pertaining to the scope of the vivarium staff, equipment and infrastructure. Qualifications Education: Bachelor's Degree in Biology, Animal Science, or related field is required
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, and humidity), accurately records environmental data and reports abnormalities to ALTIII or Supervisor. Assists the ALTIII and/or area Supervisor with vivarium support tasks including but not limited
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new research techniques and protocols. Collects, analyzes and interprets data. May assist in preparation of grant proposals. Participates in publications and presentations as author or co-author
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period. The incumbent may develop, adapt, and implement new research techniques and protocols. The incumbent analyzes, interprets data, and may assist in the preparation of grant proposals. This position
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preparation of data for publication and/or presentation at scholarly meetings, and assist in general laboratory maintenance. This position does not have supervisory responsibilities. Qualifications Primary Job