SHIRLEY RICHARDSON ALSTON
Wake Forest, NC ***** – 919-***-****
accaxk@r.postjobfree.com
SIEMENS INDUSTRY, WENDELL, NC
A Global Corporation specializing in electronics & engineering services
Administrative Support (LMV) 7/2013-9/2013
Superior Recruiting: Supported Project Manager in a Contract Administrator position
while permanent employee was on medical leave. Interacted with Director, Project Manager
and factory in Mexico to place/expedite orders. Worked with Finance to update invoicing.
Contract Administrator (LMV) 12/1/12-1/31/13
Superior Recruiting: Employment time was extended in LMV to assist Contract
Administrator for a short time with invoicing and order placement. Interacted with
Director, Project Manager and factory in Mexico to place/expedite orders.
Administrative Specialist III (EVI) 2010-2012
Reviewed and booked customer orders. Performed a wide variety of administrative and
reporting duties for Director and other key divisional management staff. Proactively
identified opportunities for improvement, proposed resolutions and integrated change
approvals.
Participated in the preparation of proposals, contracts, and other documents required by
customers in the bid process
Directed interactions between Business Developers, Warehouse logistics, and Project
Management office for changes in order status to ensure timely customer communication.
Participated in weekly backlog updates meetings and reported outcome to upper
management
Validated Salesforce.com opportunities to ensure current sales activity/records
Sales Assistant 2010-2010
Provided clerical support to the Director of PRO SYS EA, Sales Manager, Operations
Manager, Manager of Marketing, Proposal Manager, and Controller.
Audited time cards in SAP to confirm all time had been recorded for each
Developed expense reports for Management staff
Responsible for travel arrangements for Management staff
GLAXOSMITHKLINE PHARMACEUTICALS (RESEARCH TRIANGLE PARK, NC)
A Global Pharmaceutical Company
Clinical Study Associate 2004-2009
Provided operational support in clinical studies conducted in the United States
Responsible for delivery of assigned studies on time and with in budget through both
internal and external sourcing strategies for site initiation
Served as operational single point of contact for study start up and site closure
Partnered with Study Manager to track project budget
Regulatory Associate 1998-2004
Facilitated discussion groups on electronic submission documentation requirements with
client groups, submission planning groups and project teams
Prepared NDAs, ADAs, Annual Reports, and tracked technical changes for FDA
submissions
UNIVERSITY OF PENNSYLVANIA (PHILADELPHIA, PENNSYLVANIA)
Research Coordinator 1992-1998
Managed daily operations and activities related to seven research grants totaling over
$12 million
Processed and monitored financial expenditures costing over $600 million
Supervised two office assistants
Facilitated all meetings for grant participants
.
EDUCATION
B.A. Business Management, Cabrini University (Radnor, PA); May 2001
Certificate, Quality Assurance/Regulatory Affairs, Temple University (Philadelphia, PA);
May 2003
COMPUTER SKILLS
Salesforce.com, SAP, MS Word, Excel, PowerPoint, MS Outlook, EZ-Suite, Damex, Web Tool,
Share point, and MS Explorer