| Distance: | Resume alert | Resumes 361 - 370 of 638 |
Management Office
Washington, DC
... September 21/2015 – July 31/2016 FDA Docket Management Office Record Clerk Summary of duties: Prepared FDA documents for scanning. Doing Quality control on the scanned file and scanned the missing pages. Uploaded the scanned documents (pdf) on the ... - 2017 Oct 05
... September 21/2015 – July 31/2016 FDA Docket Management Office Record Clerk Summary of duties: Prepared FDA documents for scanning. Doing Quality control on the scanned file and scanned the missing pages. Uploaded the scanned documents (pdf) on the ... - 2017 Oct 05
Project Clinical Research
Lanham, MD, 20706
... Documentation Management TMF Auditing/ Management Monitoring Reports/ Clinical Study Forms Quality Assurance Audits FDA Audit Issues/ Guidelines CTCAE/ RECIST Criteria Technical Competencies Operating Systems: Mac OXX, Windows 9x/NT/200/XP ... - 2017 Oct 03
... Documentation Management TMF Auditing/ Management Monitoring Reports/ Clinical Study Forms Quality Assurance Audits FDA Audit Issues/ Guidelines CTCAE/ RECIST Criteria Technical Competencies Operating Systems: Mac OXX, Windows 9x/NT/200/XP ... - 2017 Oct 03
Engineering Project Scheduling
Silver Spring, MD
... FDA, OSHA, NDA, PA/NJ Dept. of health Insurance Carriers with no significant citations. Analyze program activities, such as acquisition or program planning, other tasks related to Government programs, weapon systems, or similar complex programs ... - 2017 Sep 30
... FDA, OSHA, NDA, PA/NJ Dept. of health Insurance Carriers with no significant citations. Analyze program activities, such as acquisition or program planning, other tasks related to Government programs, weapon systems, or similar complex programs ... - 2017 Sep 30
******@***.***, 571-229-0654
Bristow, VA
... and other required study documentation Act as a mentor for new clinical staff and may provide assistance to the CTL as designated Clinical Research Associate Performs clinical monitoring in compliance with FDA regulations and all related SOPs. ... - 2017 Sep 29
... and other required study documentation Act as a mentor for new clinical staff and may provide assistance to the CTL as designated Clinical Research Associate Performs clinical monitoring in compliance with FDA regulations and all related SOPs. ... - 2017 Sep 29
Nurse Practitioner Registered
Hyattsville, MD
... evaluate healthy volunteers, blood donors, and research patients for apheresis and phlebotomy procedures in accordance with FDA/AABB regulatory guidelines, as well as standard operating procedures Proficient in Autologous and Allogeneic transfusable ... - 2017 Sep 09
... evaluate healthy volunteers, blood donors, and research patients for apheresis and phlebotomy procedures in accordance with FDA/AABB regulatory guidelines, as well as standard operating procedures Proficient in Autologous and Allogeneic transfusable ... - 2017 Sep 09
Safety Support
Washington, DC
... Responsible for Archival of FDA 15-Day reports •Responsible for printing and mailing follow-up letter to Health Care Professionals, Consumers and letter to other company via faxing or sending via email address, converting word documents into PDF •As ... - 2017 Sep 07
... Responsible for Archival of FDA 15-Day reports •Responsible for printing and mailing follow-up letter to Health Care Professionals, Consumers and letter to other company via faxing or sending via email address, converting word documents into PDF •As ... - 2017 Sep 07
Data Management
Arlington, VA
... Analysis and improvement of import screening technology for FDA using SPSS and SAS. This involved the use of text mining, rules engine modification, clustering and taxonomy management. Creation and implementation of a performance testing plan for ... - 2017 Aug 17
... Analysis and improvement of import screening technology for FDA using SPSS and SAS. This involved the use of text mining, rules engine modification, clustering and taxonomy management. Creation and implementation of a performance testing plan for ... - 2017 Aug 17
Customer Service Pharmacy
Springfield, VA
... Dispensed medications according to all regulatory policies and procedures to include but not limited to: - Drug Enforcement Administration (DEA), State Board of Pharmacy, HIPAA, Principles of Responsibility, and FDA etc. 5/1/1995 - 04/1/1996 Potomac ... - 2017 Aug 08
... Dispensed medications according to all regulatory policies and procedures to include but not limited to: - Drug Enforcement Administration (DEA), State Board of Pharmacy, HIPAA, Principles of Responsibility, and FDA etc. 5/1/1995 - 04/1/1996 Potomac ... - 2017 Aug 08
Project Manager
Rockville, MD
... Nov 2009 – March 2017 Client (On-Site): Food and Drug Administration (FDA) Primary Role: IT Project Manager & Product Owner Manage full lifecycle projects following the SDLC framework including development, integration, testing, training, deployment ... - 2017 Jul 29
... Nov 2009 – March 2017 Client (On-Site): Food and Drug Administration (FDA) Primary Role: IT Project Manager & Product Owner Manage full lifecycle projects following the SDLC framework including development, integration, testing, training, deployment ... - 2017 Jul 29
State University Research
Silver Spring, MD
... Eighteen years in laboratory research experience in the bio/pharmaceutical industry in compliance with GLP, FDA, AAALAC and OECD guidelines. Eighteen years in vivo animal model development in areas of bacteriology, ophthalmology and oncology. Ten ... - 2017 Jul 18
... Eighteen years in laboratory research experience in the bio/pharmaceutical industry in compliance with GLP, FDA, AAALAC and OECD guidelines. Eighteen years in vivo animal model development in areas of bacteriology, ophthalmology and oncology. Ten ... - 2017 Jul 18