High energy professional with exceptional interpersonal, communication and leadership skills. Resourceful, creative and loyal.

COMPANY	POSITION HELD	DATES WORKED
(Confidential)	Protocol Associate	4/2007 - Present
Chrysler Financial	Accounts Manager	5/2002 - 6/2006
Marriott Hotel	Recruiter for Human Resources	1/1999 - 5/2002

SCHOOL	MAJOR	YEAR	DEGREE
University of Phoenix	Health Administration	2010	Master Degree
Temple University	Busniness Management/Marketing	2002	Bachelor Degree

Highlights:

My current employer has given me two awards. The first award is for outstanding service and the second award is for outstanding teamwork.

Companies I like:

Hospitals, CRO

P&L responsibilities
Presentation
Ecommerce Strategy and digital marketing channels optimization - SEO, SEM, email, affiliates - for high-profile accounts.
Technology Solutions
Sales Support
Software Implementation
Requirements Analysis & Specification
Leadership
Oracle Management System/Clinical Trials Management System, Outlook, Website Maintenance, Powerpoint, Access, Go to Webinar/Meeting, Survey Monkey, Citrix, MS Word, MS Excel and Case reimbursement processing

• Oracle Management System
• Citrix
• Case Reimbursement
• Website Maintenance
• Access

Provide protocol support to the Protocol Manager and administration department by preparing and moderating conference calls and meetings for trials and committee chairs. I also maintain protocol accuracy among members and files by updating regulatory documents such as SOP’s and Work Instructions wherever needed along with updates to the website. I develop and manage presentations for quarterly meetings, create and revise systems and procedures, report and process case reimbursements for medical sites involved with the protocols as needed. I provide support in creating the annual budget for continuing grants. Provide customer service to internal staff and participating sites, monitor site recruitment materials (IRB approvals, Protocol Specific Applications, Scanning Qualifications, etc.) to ensure site readiness for specific trials and GCP standards, work with other departments such as Data Management, Regulatory compliance, Medical writing and Imaging to make certain that communication remains consistent across all fields. In addition, I accompany and assist in the semi-annual meetings off site. I have been involved with clinical trials such as CQIE, NOPR and RESCUE.