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Resume alert |
Resumes 21 - 30 of 737 |
Sterling, VA
... Support OIMT IT Governance activities pertaining to FDA’s CPIC Program Support the development of presentation materials and regulatory reporting activities to FDA’s Governance Boards including FDA’s Technology Council, Portfolio Review Board (PRB) ...
- Mar 14
Silver Spring, MD
... and Administrator (August 2017 – Present) Food and Drug Administration (FDA), Maryland •Developed and maintained SharePoint online hub sites, associated sites, lists, libraries, pages, content types, and site columns for intranet development. ...
- Mar 13
Rockville, MD
... Project scope included existing custom software applications that had been in use for several years but not properly validated according to CAPA from FDA audit findings. • Experience with Legacy System -Data Migration. • Participated in an in-house ...
- Mar 08
Elkridge, MD
... 2021 ASSOCIATE GENERAL COUNSEL In house counsel at FDA-sponsored public-private partnership devoted to medical device safety and efficacy. Led initiative to build real world evidence data cloud to host global health data. Advised on privacy and ...
- Mar 04
Crofton, MD
... proposal efforts Key Highlights Successfully produced proposals to DOD, NASA, DOL, DOS, DOJ, IRS, FDA, FAA and others covering IT Support services, Cybersecurity, Data Center, Program Management, Cloud Services, Big Data Analytics, Call Centers etc. ...
- Feb 29
Riverdale Park, MD, 20737
... predictive models for outcome forecasting •Ensured organizations' compliance with regulatory requirements, including HIPAA, GDPR, and FDA regulations, safeguarding data privacy and integrity •Ensuring that healthcare organizations are compliant with ...
- Feb 25
Washington, DC
... Directed safety operations and maintained clean work environment to adhere to the Food and Drug Association (FDA) and the Occupational Safety and Health Administration (OSHA) requirements. Developed and maintained professional functional working ...
- Feb 19
Downtown, DC, 20004
... All protocols were based on FDA laws, regulations and standard. Responsibilities also included contributions to science and participating in Institutional Review Board (IRB) meetings annually. The foci of the units also included gene cognition, ...
- Feb 19
Rockville, MD
... Review Board (IRB) processes for new application submissions, amendments, and continuing reviews in accordance with 45 CFR Part 46 – Protection of Human Subjects, document compliance to the 2018 Common Rule, and FDA regulatory requirements. ...
- Feb 17
Downtown, DC, 20004
... ● Developed an AI-driven innovative end-to-end prescription solution that analyzes a patient’s clinical history, FDA drug database, and standard of care guidelines to generate unique patient-specific recommendations. ● Built a system Integrated with ...
- Feb 16