| Resume alert | Resumes 51 - 60 of 192 |
Clinical Research Manager
Great Falls, VA, 22066
... knowledge of FDA regulatory requirements and ICH/GCP guidelines. Highly adept at creating and reporting metrics on project management, tracking records, and performance. Developed and executed strategic projects that have improved operational ... - 2020 Oct 31
... knowledge of FDA regulatory requirements and ICH/GCP guidelines. Highly adept at creating and reporting metrics on project management, tracking records, and performance. Developed and executed strategic projects that have improved operational ... - 2020 Oct 31
Junior Compliance Analyst
Fairfax, VA
... – Contractor for FDA, CTP Selected to investigate tobacco events in the United States for the potential distribution of free samples and compile a weekly report for the Center for Tobacco Products (CTP) Examine and evaluate labels, advertisements, ... - 2020 Oct 28
... – Contractor for FDA, CTP Selected to investigate tobacco events in the United States for the potential distribution of free samples and compile a weekly report for the Center for Tobacco Products (CTP) Examine and evaluate labels, advertisements, ... - 2020 Oct 28
Oracle Support
Germantown, MD
... Consultant This project involved in the support and maintenance of Unified Financial management system (UFMS) for HHS and its OpDivs FDA, CDC, HIS and PSC to offer effective processing and tracking of financial and accounting transactions. ... - 2020 Oct 20
... Consultant This project involved in the support and maintenance of Unified Financial management system (UFMS) for HHS and its OpDivs FDA, CDC, HIS and PSC to offer effective processing and tracking of financial and accounting transactions. ... - 2020 Oct 20
Engineer Manager
Germantown, MD
... mobile automation testing Artech/Independent Contractor 10/2017 - 09/2018 Expert Consultant Responsibilities: · Performing IV&V Quality Management assessments for Legacy and NexGen modernization system for the FDA Center for Tobacco Products (CTP). ... - 2020 Oct 13
... mobile automation testing Artech/Independent Contractor 10/2017 - 09/2018 Expert Consultant Responsibilities: · Performing IV&V Quality Management assessments for Legacy and NexGen modernization system for the FDA Center for Tobacco Products (CTP). ... - 2020 Oct 13
Food Assistant
Centreville, VA
... Kelly Food Science Award for Excellence FDA/USDA Certification for thermal processing of canned foods HACCP Certification USFSA Double Gold Medalist in Ice Dance and Moves in the Field - 2020 Oct 08
... Kelly Food Science Award for Excellence FDA/USDA Certification for thermal processing of canned foods HACCP Certification USFSA Double Gold Medalist in Ice Dance and Moves in the Field - 2020 Oct 08
Business Analyst
Ashburn, VA
... Managed a team of six individuals to successfully implement a Regulatory management system to improve company efficiency and FDA compliance Devised a communication strategy for the team and analyzed system modifications requested by users to be ... - 2020 Oct 05
... Managed a team of six individuals to successfully implement a Regulatory management system to improve company efficiency and FDA compliance Devised a communication strategy for the team and analyzed system modifications requested by users to be ... - 2020 Oct 05
Clinical Research Medical
Herndon, VA
... of new QAA staff Acquiring working knowledge of the technical concepts required for PV Auditing Acquiring knowledge of FDA, EMeA and other international Quality System rules and regulations Acquiring knowledge of pharmaceutical/biotechnology ... - 2020 Oct 05
... of new QAA staff Acquiring working knowledge of the technical concepts required for PV Auditing Acquiring knowledge of FDA, EMeA and other international Quality System rules and regulations Acquiring knowledge of pharmaceutical/biotechnology ... - 2020 Oct 05
Sas Programmer
Fairfax, VA
... ●Experience in analyzing and coordinating clinical data, generating detailed summary reports and data validation using FDA regulation procedures. ●Supported for trial feasibility analysis for oncology and other key therapeutic areas for all Phases. ... - 2020 Oct 05
... ●Experience in analyzing and coordinating clinical data, generating detailed summary reports and data validation using FDA regulation procedures. ●Supported for trial feasibility analysis for oncology and other key therapeutic areas for all Phases. ... - 2020 Oct 05
Student
Sterling, VA
... oFamiliarized with FDA and ISO standards for medical devices. 3-D Biomechanical Eye Modeling Using Patient-Specific MRI Images JAN 2019 – MAY 2020 ●Constructing 3D biomechanical eye models and using them to quantify specific morphological parameters ... - 2020 Aug 13
... oFamiliarized with FDA and ISO standards for medical devices. 3-D Biomechanical Eye Modeling Using Patient-Specific MRI Images JAN 2019 – MAY 2020 ●Constructing 3D biomechanical eye models and using them to quantify specific morphological parameters ... - 2020 Aug 13
Assistant Clinical Research
Germantown, MD
... Digene Corporation, Gaithersburg, MD (Permanent) Administrative Assistant, March 2003 June 2005 Assisted with the company’s preparation for their FDA Panel Review for the company’s Medical Device Approval. Assisting with included various components ... - 2020 Jul 16
... Digene Corporation, Gaithersburg, MD (Permanent) Administrative Assistant, March 2003 June 2005 Assisted with the company’s preparation for their FDA Panel Review for the company’s Medical Device Approval. Assisting with included various components ... - 2020 Jul 16