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for evaluation of suitability and clinical management of potential donors. Formulates donor maintenance plan to preserve transplantable organs based on available clinical knowledge. Ensures that organs
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visits in a timely manner. Ensures data integrity and consistency in computer database and written records by reviewing entered data for accuracy. Execute the plan developed for collection of protocol
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to the Islet Distribution Program. Actively participate in the design and execution of experimental R&D initiatives to improve current technologies and methodologies used in the human cell processing facility
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, ventilator/respiratory care, clinically significant medical ailments, disease process, infection control, etc. Acts as clinical support resource to DMC I and Designated Requestor/Referral Responder as needed
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Summary (AVS) for post-visit instructions and checkout orders for testing by coordinating program activities with other programs, departments, or staff to ensure optimum efficiency. Assist in the management
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Attitudes: Ability to communicate effectively in both oral and written form. Skill in completing assignments accurately and with attention to detail. Ability to process and handle confidential information
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assist the Research Program Leaders to prepare for External Reviews and Advisory Boards. These reviews are critical for the successful development of all the Programs. The Reviews require coordination with
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healthcare professionals related to assigned patients to assess, plan, implement and evaluate patient care plans. 4. Prepares patients for, and assists with examinations, procedures and treatments. Considers
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operational initiatives with institutional goals. Identifies growth opportunities, assesses market trends, and supports new program development through data-informed planning. Oversees the design
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for structure-based and ligand-based drug design. ● Utilize computational tools to predict and optimize pharmacokinetic (PK) and pharmacodynamic (PD) properties of drug candidates. ● Design and implement