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and Responsibilities: Performs a variety of project-specific process development tasks for multiple clients following standard operating procedures (SOPs). Maintains good documentation in laboratory
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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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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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(AAALAC) site visits, and semi-annual Institutional Animal Care and Use Committee (IACUC) inspections for the husbandry, operations and facility programs. Develops procedures for continuous process
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research activities involving all aspects of the research process, to include, but not limited to; investigation, technical, testing/validation of results, and report findings. The Associate will perform a
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: Performs a variety of project-specific process development tasks for multiple clients following standard operating procedures (SOPs). Maintains good documentation in laboratory notebooks, data record
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. Observes and follows safety standards and procedures. Department-Specific Responsibilities: Process, aliquot, store, and track human biological specimens, including blood, cerebrospinal fluid (CSF), plasma
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programming and equipment testing and measurement. Physical Demands: Standing, Walking, Sitting, Lifting 50 lbs. Carrying 50 lbs. Pushing 50 lbs. Pulling 50 lbs. Reaching, Handling, Grasping, Feeling, Talking
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. Excellent communication (written and verbal) skills. Background in medical statistics and computer science (preferred). Physical Demands: Able to perform moderate lifting. Able to sit, stand and walk
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, Sociology or related degree preferred Licenses: - CPT- Phlebotomy Certification license required Experience: 1 year clinical research experience preferred Physical Demands: - Able to perform moderate lifting