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: Recognizes when typical agreements (MTAs, CDAs, DUAs, DTAs, etc.) are necessary and alerts appropriate parties. Prepares FDA regulatory submissions in collaboration with ORAQ, including development, submission
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study documentation, protocol submissions, and SOPs. May train others in these policies and processes. Is responsible for all aspects of managing and documenting Investigational Product (IP); including
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. May train others. Prepares for and provides support for study monitoring and audit visits, including support for the reviewer. Addresses and corrects findings. May train others. Maintains all
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, Medrio, and Veeva Vault EDC systems Experience preparing data for monitoring visits, audits, and study closeout Ability to train or mentor junior research staff Other Requirements Ability to work in
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Be You. At Duke, we celebrate individuality and the unique perspectives that each member of our community brings. As the Director, Healthcare Facility Security, you will collaboratively develop
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are proud to have met the challenge of accreditation and intend to consistently uphold the principles of quality improvement in patient care. Learn more here: https://www.dukehealth.org/locations/duke
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, documentation, and analysis of clinical research data. May oversee the work of junior staff and train or mentor others in clinical research tasks. Work Performed Research Operations Recognizes when typical
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Associate in Research The role involves developing and optimizing machine learning models to predict infectious diseases using multimodal health data. Responsibilities include analyzing correlations between
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development, knowledge sharing, and a network of fellow project planners. Minimum Requirements Bachelor’s degree. Two years of experience in project management with increasing scope and independence
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, document and draw tentative conclusions from experimntal results. Confer with principal investigator to review work assignments and develop plans for research experiments; make minor modifications