| Distance: | Resume alert | Resumes 341 - 350 of 634 |
Data Sas
Herndon, VA, 20170
... Experience in analyzing and coordinating clinical data, generating detail summary reports and data validation using FDA regulation procedures. Extensively involved in SAS clinical trails &data analysis and preparation of SAS Data sets, Reports, ... - 2018 Feb 09
... Experience in analyzing and coordinating clinical data, generating detail summary reports and data validation using FDA regulation procedures. Extensively involved in SAS clinical trails &data analysis and preparation of SAS Data sets, Reports, ... - 2018 Feb 09
Analyst
Chevy Chase Village, MD, 20815
... funded project from USCIS, and lead a team of undergraduate researchers working on another government funded project for the FDA and was recognized as a contributing author on several deliverables to these funding agencies • Peer Mentored seven ... - 2018 Feb 06
... funded project from USCIS, and lead a team of undergraduate researchers working on another government funded project for the FDA and was recognized as a contributing author on several deliverables to these funding agencies • Peer Mentored seven ... - 2018 Feb 06
Medical writing/editing, clinical research, project management
Silver Spring, MD
... implemented CME proposals, developed needs assessments (gap analysis, evidence, learning objectives) Analyzed and developed FDA guidelines, scientific meeting minutes, and Quick Review reports Outreach to Minority Populations and Patient Advocacy ... - 2018 Feb 01
... implemented CME proposals, developed needs assessments (gap analysis, evidence, learning objectives) Analyzed and developed FDA guidelines, scientific meeting minutes, and Quick Review reports Outreach to Minority Populations and Patient Advocacy ... - 2018 Feb 01
Biomedical Engineer
College Park, MD
... Food and Drug Administration (FDA), CDRH, Silver Spring July 2017 – September 2017 o Researched state-of-the-art mock circulatory loop (MCL) technologies. o Researched clinical patient data and created customized target input waveforms for MCL by ... - 2018 Jan 13
... Food and Drug Administration (FDA), CDRH, Silver Spring July 2017 – September 2017 o Researched state-of-the-art mock circulatory loop (MCL) technologies. o Researched clinical patient data and created customized target input waveforms for MCL by ... - 2018 Jan 13
Biopharmaceutical Manufacturing Associate
Washington, DC
... Performed Lead staff and management duties –allocated staff and resources to ensure compliance with FDA, ensured teams worked cohesively while meeting strict timelines, sent out daily updates to senior management; Provided on-the-floor supervision ... - 2018 Jan 10
... Performed Lead staff and management duties –allocated staff and resources to ensure compliance with FDA, ensured teams worked cohesively while meeting strict timelines, sent out daily updates to senior management; Provided on-the-floor supervision ... - 2018 Jan 10
d
Rockville, MD
... Qumas (E-Document Compliance)/ FDA approved Plateau Learning Program (MyLearning)/ FDA approved QLIMS (Quality Control Computer-based program)/FDA approved Proficient at using general laboratory equipments Work well as team member or independently. ... - 2018 Jan 10
... Qumas (E-Document Compliance)/ FDA approved Plateau Learning Program (MyLearning)/ FDA approved QLIMS (Quality Control Computer-based program)/FDA approved Proficient at using general laboratory equipments Work well as team member or independently. ... - 2018 Jan 10
Office Management
Fort Washington, MD
... Clearance Level Level 5 Public Trust Clearance (Obtained February 2008 at FDA through Northrop Grumman) Summary of Qualifications Over 5 years in the Federal and Business industry with IT and Administrative experience in: Personnel coordination, ... - 2018 Jan 08
... Clearance Level Level 5 Public Trust Clearance (Obtained February 2008 at FDA through Northrop Grumman) Summary of Qualifications Over 5 years in the Federal and Business industry with IT and Administrative experience in: Personnel coordination, ... - 2018 Jan 08
Medical Manager
Silver Spring, MD
... * Real time PCR detection of HPV 16.18.31.6,11 particles from Larvag samples * Completed 12000 patients samples study from worldwide for safety, efficacy study * Ensure all clinical sample test records and documents completion for FDA inspection ... - 2018 Jan 07
... * Real time PCR detection of HPV 16.18.31.6,11 particles from Larvag samples * Completed 12000 patients samples study from worldwide for safety, efficacy study * Ensure all clinical sample test records and documents completion for FDA inspection ... - 2018 Jan 07
Management Manager
Potomac, MD
... Provided microbiological audits of environmental microbiological testing and responded to FDA 483s. Just completed a 7 weeks consultation for environmental microbiological issues in a pharmaceutical plant in Long Island, NY under the aegis of ... - 2017 Dec 31
... Provided microbiological audits of environmental microbiological testing and responded to FDA 483s. Just completed a 7 weeks consultation for environmental microbiological issues in a pharmaceutical plant in Long Island, NY under the aegis of ... - 2017 Dec 31
State University Engineering
Lorton, VA
... bench testing, prototyping, and pre-clinical trials while considering FDA & ISO documentation & standards • Expert in electrochemical biosensor and immunosensor research and development • Knowledgeable in data and statistical analysis (e.g. ... - 2017 Dec 22
... bench testing, prototyping, and pre-clinical trials while considering FDA & ISO documentation & standards • Expert in electrochemical biosensor and immunosensor research and development • Knowledgeable in data and statistical analysis (e.g. ... - 2017 Dec 22