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Resumes 281 - 290 of 638 |
Rockville, MD
... Provide a medical opinion regarding medical based questions, legal and regulatory matters, based on the CMS regulations, FDA regulations, HIPAA compliance Provide a communication between clinicians, researchers and IT specialists involved in the ...
- 2020 Apr 12
Vienna, VA
... Client: FDA Alfresco Customization/Development for FDA CSTAR(Center Submission Tracking and Reporting) Developing custom model in alfresco which includes customization of Aspects/Permissions/Behavior model of the system. Developing custom Datalists ...
- 2020 Apr 10
Washington, DC
... Prepared technology transfers documents, protocols and SOPs for regulatory submission to FDA-CBER. Developed a process to manage data reporting clinical records for Post- Marketing Surveillance Study. 1997-1997 GLAXOSMITHKLINE, Inc., Raleigh, NC, ...
- 2020 Apr 05
College Park, MD
... correctly with 96% accuracy Center for Health Information and Decision Systems Research (Artificial Intelligence in Drug Development) Dec 2019 – Present Analysed the FDA’s perspective towards incorporation of AI in Drug development and healthcare. ...
- 2020 Apr 05
Centreville, VA
... and Software Engineers consultants ●Support agencies such as FBI, CIA, NRO, DIA, ODNI, TSA, NASA, DARPA, DOE, DOD, DHA, OPM, FDA, NCTC and DLA ●Assess needs and capture action items from hiring managers, directors, and VP’s to streamline requisition ...
- 2020 Apr 02
Rockville, MD
... These documents, which receive minimal review before transmittal from the division to the Center Director, state or interpret Center or FDA policy for the regulated industry and the medical community. Arrange and analyze monthly project tracking ...
- 2020 Mar 09
Upper Marlboro, MD
... Utilized NetIQ IAM to manage FDA environment. Recover, download, and install escrowed certificates for all users and systems requiring access to data encrypted with previous certificates Perform all network and system non-PIV Certificate issuance ...
- 2020 Mar 07
Fairfax, VA
... (submission of 1572 and FDA form, protocol Signature Pages) and update it to the Trial Master Files as needed. Carefully collect, compile and document clinical research data according to the study protocol and sponsor guidelines. Maintain ...
- 2020 Feb 10
Ashburn, VA, 20148
... Agencies include, CMS, Food Drug Administration (FDA), Centers for Disease Control and Prevention (CDC), and National Institute of Health (NIH). Healthcare projects include working with the state of West Virginia to bolster their Medicaid program, ...
- 2020 Feb 06
Washington, DC
... Deputy Program Manager (Contractor) Caelum Research Corporation 1700 Research Boulevard Suite 100 Rockville, MD 20850 Site – Government - FDA/CBER/DCC February 2002 – January 2010 (Lay - Off) Supervised 23 Employee’s performing hands on File Room ...
- 2019 Dec 27