1. DGM D e a n n a G o o d w i n M o u s e r
6254 Kraft Ave. North Hollywood, CA 91606 Cell (818) 391-7408
OVERVIEW
A high energy, individual with a proven track record for consistent, exemplary results representing
sellers and buyers. Recognized for the ability to work on multiple projects in a fast pace
environment.
EDUCATION
California State University Northridge, B.A. Degree in Sociology
University of California Los Angeles, Completion of online course in Protecting
Human Research Subjects in Biomedical and Genetics Research
California Bureau of Real Estate, California Real Estate License
SKILLS
Experience managing Phase I-IV clinical research studies focusing on efficacy and
acceptability
Knowledge applying and understanding clinical research protocols and FDA/ICH
regulations
Background working with CRO’s (Clinical Research Organizations)
Experience with Microsoft Word, Excel, Outlook, Lotus Approach, Access, SPSS,
PowerPoint, Entrypoint
PC and Apple Macintosh knowledge
EMPLOYMENT
2012 to present Keller Williams Burbank, CA
World Media Center
Licensed Agent
Successfully management with vendors to guarantee contracts are adhered to and close
on time
Monitor fulfillment of purchase contract terms to ensure that they are handled in a timely
manner
Responsible for executing and managing all documents such as contracts, purchase
agreements, disclosures, closing statements, deeds and leases
Conduct and draft comparable market analysis and reports for all clients to appraise
property values
Management of on-line files for inter-office audits utilizing “dotloop” metrics system
Coordinate contract closings, oversee signing of documents and disbursement of funds
Communicate and advise clients on prices and legal requirements
Research and conduct title searches of properties
Represent buyers, sellers, and renters negotiating on their behalf
Schedule and interview clients to assess purchase goals and wishes are met
2008 to 2011 Clinical Trials, Valencia, CA
Quest Diagnostics
(Clinical Trials, Quest Diagnostics is a central laboratory that specializes as a direct liaison
between pharmaceutical companies and sites managing laboratory testing results and storage for
drug trials outlined by study protocols. The trials are funded by major pharmaceutical or medical
device companies and NGOs.)
Project Manager
2. Break down study protocols to make sure study parameters were completely defined
Facilitate meeting with sponsors and team members to ensure that project requirements
are met
Design all study databases, requisitions and investigator manuals for sites to collect
pertinent data outlined by study protocols
Responsible for monitoring studies with Project Associates to ensure all client data is
clean and accurate
Manage all service related issues
Schedule and conduct regular meetings with sponsor and team members to discuss
problem resolutions of study specific issues
Collaborate with counterparts to ensure global consistency on global study setup
Prepare weekly study status reports
Assist in Quality Control and ensured setup of studies meet all Quality Standards
Attend and participate in all internal and client audits
2005 to 2008 Phillips Graduate Institute Encino, CA
Project Coordinator
Independent management of research project
Created annual budget and accurately keep all financial records for department
Regular contact with Institutional Review Board regarding regulatory issues and verifying
all study requirements are being appropriately completed
Developed and designed consent forms, case report forms and databases to collect and
track all data outlined by study protocol
Worked directly with Research Director on data analysis and creating database files
Documented and organized all program correspondence and study measurement tools
Coordinated, collected and edited all data for research project
Created, maintained study timelines, Standard Operational Procedure Manuals (SOP’s)
and databases
Responsible for training all staff to work on research project
1998 to 2005 California Family Health Council, Inc. Los Angeles, CA
(California Family Health Council is an organization that manages HIV and gynecologic drug
trials. It serves as an SMO, Site Management Organization, for some trials and as a CRO,
Clinical Research Organization, for other trials. The trials were funded by either NIH, NGOs,
pharmaceutical or medical device companies.)
Associate Project Director (2000-2005)
Managed several clinical research trials (Phase I-IV) from inception through clinical study
report
Worked closely with study sponsors to develop and edit protocols
Trained and Supervised team of 20 Clinical Research Associates
Created CTMS for several trials
Created database for Clinical Trial Assistant to key enter CRF data into
Designed measurement tools, source documentation templates, and CRFs for data
collection
Served as key liaison between Sponsor and sites
Reviewed and edited all incoming CRFs and source documentation
Developed monthly reports to outline project and staff progress
Responsible for clinician in-service training
Performed quality assurance checks on multiple projects
Research Assistant (1998-2000)
3. Archived all incoming data documents (Trial Master File)
Updated CTMS system and reimbursement logs
Consented participants and ensured completion of all required source documentation by
site personnel
Scheduled participants appointments
Screened and determined study participants eligibility
1996-1998 Matrix Center West Hills, CA
Researcher/Administrative Assistant
Conducted research to evaluate and assess the benefits of a cognitive behavioral
intensive outpatient program
Served as office manager with duties including account billing, deposits, payment journal
entries and filing
Responsible for managing clients charts
1996-1998 California State University Northridge Northridge, CA
Student Health Center
Program Coordinator (1997-1998)
Facilitated weekly staff meetings
Responsible for annual training of 10 peer counselors
Assisted with annual budget proposal
Wrote and updated educational materials and designed publicity materials
