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. May provide oversight or training to study team members collecting or entering data. Assists with quality control and data cleaning as directed. Independently responds to queries created by a CRO or the
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Bonus Relocation Research focused CNMT (Certified Nuclear Medicine Tech) or ARRT Nuclear Medicine (American Registry of Radiologic Technologists) Clinical Ladder State- of -the- art- technology Join the
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intersection of technology, data, and higher education administration. You will play an important role in helping the Office of the University Registrar deliver reliable information, support evidence-based
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ASSOCIATE SCIENTIST/ENGINEER I GMP Analytics – Duke Human Vaccine Institute Be You. Position Overview: The Associate Scientist I will support the development, qualification and execution of analytical methods
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, inaccurate or missing data for minimal risk studies. Follows SOPs for quality assurance. Runs summaries and reports on existing data. Follows required processes, policies, and systems to ensure data security
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Senior Policy Analyst, Duke Margolis Institute for Health Policy Hybrid (Washington DC or Durham NC)
engineering, and fosters extensive relationships with stakeholders both internal and external. These relationships span foundations, private sector organizations, state and federal governments, and global
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Senior Policy Analyst, Duke Margolis Institute for Health Policy Hybrid (Washington DC or Durham NC)
engineering, and fosters extensive relationships with stakeholders both internal and external. These relationships span foundations, private sector organizations, state and federal governments, and global
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the next generation of nursing professionals. Be You. The Duke University School of Nursing is seeking a skilled and service‑driven Information Services Specialist to join our technology team. In this role
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ability to handle multiple assignments simultaneously, technology skills, medical terminology, and understanding of clinical medicine. Must be able to flex with the demand of work schedules and timelines
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Quality (ORAQ), including development, submission, and maintenance of relevant documentation. Addresses FDA review and potential hold issues in collaboration with the PI. Knowledgeable in regulatory and