Orthopedic Ultrasound Neurosurgery ENT Vascular Microsoft Office Spanish XP Microscopes Medical Devices Surgery Clinical Research Software Windows Medical Imaging Positive Can-do Attitude Team-orientated Customer-focused Customer Service Customer Profitability Sales
Jan 2012 to Present Financial ConsultantShore Alternative Investment Consulting, LLC Rumson, NJ Jan 2011 to Dec 2011 PrincipalResolution Partners, LLC New York, NY Apr 2007 to Jun 2009 Director, Risk ManagementGottex Fund Management New York, NY Jul 2005 to Apr 2007 Senior Associate, Operational Due DiligenceClinton Group Inc
Sep 2003 to Apr 2004 Director, Special ProjectsClinton Group Inc
Aug 2000 to Sep 2003 Director, OperationsClinton Group Inc
May 1998 to Aug 2000 Portfolio ManagerClinton Group Inc
Oct 1996 to May 1998 AnalystGoldman Sachs and Co., Inc New York, NY Feb 1994 to Oct 1996 Consultant, Controllers Department of Commodities DivisionProfessional Golf Course Management Fair Haven, NJ Oct 1991 to Jan 1994 Financial Analyst
Education:
Monmouth University West Long Branch, NJ May 1991 Bachelor of Science in Business Administration
Dr. Moran graduated from the Marshall University Edwards School of Medicine in 2004. He works in Fort Gay, WV and specializes in Internal Medicine. Dr. Moran is affiliated with Cabell Huntington Hospital and St Marys Medical Center.
Us Patents
Process For Making A C6 To C12 Dibasic Acid Or Azelaic Acid Using Ozone Generated From Carbon Dioxide
Samuel Lane - Kennett Square PA, US Edward Moran - Gibbstown NJ, US John Ostermaier - Wilmington DE, US
International Classification:
C07C031/18 C07C027/02
US Classification:
568/852000, 568/876000, 568/877000
Abstract:
Disclosed is a method for preparing a substantially pure mixture of cyclododecanediol isomers. The isomers include 1,4-cyclododecanediol, 1,5-cyclododecanediol, and 1,6-cyclododecanediol. Also disclosed is a method for using a substantially pure mixture of cyclododecanediol isomers, which include the preparation of diamines; esters; diesters, such as diacetates and diacrylates; bis-phenol cyclododecane; and cyclododecanediol-based polyester polymers and polyester polyols.
Edward F. Moran - Moorestown NJ Harold A. Hartung - Collingswood NJ
International Classification:
C05F 1102
US Classification:
71 24
Abstract:
Peats, mucks, soils, anaerobic sludges, lignites and other humus materials containing humic substances are slurried in the natural wet state with additional water at low pH to free humic acid from salts it may have formed in the natural state and to disperse the humic acid as a fine suspension in the water. The resulting slurry is then screened to remove coarse material such as stones, fibers and cellulosic materials that may be present, and the liquid phase compromising a dispersion of humic acid is settled or otherwise treated to remove heavy inorganic fines if present. The dispersion is then filtered to yield a relatively pure and dry filter cake, comprising crude humic acid. This product may be converted to soluble humate salts by adding a solubilizing agent such as sodium hydroxide, separating residual insolubles and drying the concentrated solution. In the alternative, the solution before drying may be converted to relatively pure humic acid by acidifying the solution, separating and drying the insoluble humic acid. The same solution may be converted to humates of limited solubility by reaction with suitable metal salts, and again separating and drying the product.
Separation Of Nylon 6 From Mixtures With Nylon 6,6
E. I. Du Pont de Nemours and Company - Wilmington DE
International Classification:
C07C 4528
US Classification:
568309
Abstract:
Preparation of 4-phenylquinol by oxidation of biphenyl using an aqueous mixture of cerium methanesulfonic acid in which the ratio of cerous to ceric methanesulfonic acid is in the rate of 0. 2 to 50 mole percent.
Edward F. Moran - Gibbstown NJ Ronald J. McKinney - Wilmington DE
Assignee:
E. I. Du Pont de Nemours and Company - Wilmington DE
International Classification:
C07C 5514
US Classification:
562590
Abstract:
Waste nylon 6 and/or nylon 6,6 are converted to adipic acid monomer by depolymerization with an aliphatic monocarboxylic acid to form alkylamides followed by oxidation of the alkylamides to adipic acid.
Youtube
St. Patrick's Day Savannah River Tugs 1
Rainy day on the River - tugboats out for some fun. This is the Edward...
Category:
Entertainment
Uploaded:
18 Mar, 2010
Duration:
2m 37s
Moran's Remarks from Cap and Tax Hearing
Congressman Jerry Moran gave remarks during a House Agriculture Commit...
Category:
News & Politics
Uploaded:
12 Jun, 2009
Duration:
6m 35s
Pin Up Hairstyle-Earl Moran Inspired...Forma....
For those of you who asked for something vintage inspired that would s...
Category:
Howto & Style
Uploaded:
13 Jul, 2009
Duration:
3m 20s
Ed Byrne slates Alanis Morissette
The now infamous slating of Alanis Morissette's 'Ironic' by Irish come...
Category:
Comedy
Uploaded:
11 Sep, 2006
Duration:
5m 3s
INMA World Congress: An interview with Edward...
Deloitte's annual Media Democracy Survey provides unique insights in e...
Category:
Nonprofits & Activism
Uploaded:
17 May, 2009
Duration:
5m 34s
Googleplus
Edward Moran
Work:
VSE Corporation - Aircraft Mechanic II (6)
Education:
University of Phoenix Axia College - Computer Science
Tagline:
Enforcer at PAX, Avionics tech by trade. Gonna make video games one day.