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Resumes 91 - 100 of 635 |
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, ...
- Jan 15
Upper Marlboro, MD
... Verify the requested hardware or software has received prior approval for use within the FDA infrastructure. Process request for Center staff for special use mailboxes, Network share access approval, Iron Key activations, distribution list, shared ...
- Jan 08
Oakton, VA, 22124
... Public Trust security clearance PROFESSIONAL EXPERIENCE Management Consultant Eagle Hill Consulting 2023 - 2024 FDA Center for Biologics Evaluation and Research (CBER) Responsible for leading internal employee engagement and executive communications ...
- Jan 02
Fort Washington, MD
... TISTA Jul 2017 – Dec 2017 Science and Technology Corporation – Rockville, MD Senior Business Analyst Maintained quality control over all business requirements for FDA's Project Management Support (PMS), ensuring adherence to documented processes, ...
- 2024 Dec 28
Vienna, VA
... Deputy Lead/Workstream Lead, Communications 2/2023 – 5/2024 EAGLE HILLL CONSULTING AT THE FOOD AND DRUG ADMINISTRATION (HHS), WHITE OAK, MD Led internal communication projects, working with leadership at FDA’s Center for Drug Evaluation and Research ...
- 2024 Dec 27
Ashburn, VA
... on the PTC Integrity, EPIC, Tele-health Project (End to End calling, audio, video support from both the parties), created Request for Change (RFC’s) in Service Now & Business/Functional Requirements for both financial /clinical (FDA) user groups. ...
- 2024 Dec 16
Washington, DC
... SAP, eLIMS, Trackwise, Docspace, Sharepoint, Veeva RIM) o Have experience in creation, review and approval of analytical stability reports and submission to US FDA / different regulatory agencies. o CAPA Support, Regulatory technical documentation. ...
- 2024 Dec 02
Silver Spring, MD
... implementation of FDA rules and regulations as required for pharmaceutical brand advertising - Expert level fact-checking and annotation in peer review to ensure comprehensive and accurate support for drug claims after licensed approval for use - ...
- 2024 Nov 23
Sterling, VA
... (SFDC) Regulations/Compliance JAWS, HIPAA, EDI Transactions (835, 837 (X-12 & Non X-12), 270/271,276/277), FDA 21 CFR 11/868/880, ISO 13485, SEC, IRS SECURITY CLEARANCE Public Trust Clearance for Centers for Medicare and Medicaid Services (CMS). ...
- 2024 Nov 20
Capitol Heights, MD
... • Familiar with the FDA 21CFR Part 11 rules and regulations. • Working knowledge of Technical Document format. BeyondAResume Contractor for Bioqual Inc. Rockville, MD 20850 Document Quality Control Coordinator/Manager 06/2021 – 12/2021 Supervisor ...
- 2024 Nov 17