Marilyn Kaye Mowrey is seeking a full-time position in clinical data management or clinical database programming. She has over 15 years of experience in establishing policies and procedures for data management, database design, database validation, data cleaning, and creation of standard and ad hoc reports. Her experience includes positions at ReliantHeart, Autonomic Technologies, Covidien, EnteroMedics, Transoma, and Eminent Research/PPD Medical Device where she developed clinical research databases, cleaned data, programmed reports, and assisted with data analysis and annual reports to the FDA. She has a Bachelor of Science in IT with a database emphasis from Kaplan University and has taken online courses in statistics, biostatistics

1. Marilyn Kaye Mowrey
1502 Quebec Ave N  Champlin, MN 55316
Phone: 763-227-0534  E-mail:kayemowrey@gmail.com
Job Objective
Seeking a full-timeclinical data management or clinical databaseprogrammer position.I haveexperience in establishing
policies and procedures for data management, databasedesign,databasevalidation, data cleaning, creation and
programming of standard and ad hoc reports, assistingwith data analysisfor abstractsand assistingwith data for annual
reports to FDA.
Experience
ReliantHeart, Inc., Remote/home-based position. January 2016 – Present
Clinical Data Manager.
Responsibilities:Clean data to ensure data integrity and lock clinical research data usingthe iMedNet EDC system. Program
standard and ad hoc reports usingthe iMedNet EDC reporting tool for trial management. UsingExcel and Stata, analyzeand
trend data as appropriate.UsingStata, Excel and Word, create annual reports for the Federal Drug Administration,as well as
summary reports for the Clinical Events Committee and Data Safety Boards. Programand test new databases in the
ClindexLiveapplication for European studies.
Autonomic Technologies, Remote/home-based position. March 2013 – December 2015
Sr. Clinical Data Manager.
Responsibilities:Develop and programclinical research databases usingClindexLiveusingSybasedatabasebackend. Clean
data to ensure data integrity and lock clinical research data usingtheSybase-based Clindex EDC system. Programstandard
and ad hoc reports usingSybaseInfoMaker. UsingExcel and Stata, analyzeand trend data as appropriate.UsingStata, Excel
and Word, create annual reports for the Federal Drug Administration,as well as summary reports for the Clinical Events
Committee and Data Safety Boards.
Covidien, Remote/home-based contractposition. March 2012 – March 2013
DatabaseProgrammer/Report Writer.
Responsibilities:Develop and programclinical research databases usingClindex.Programstandard and ad hoc reports using
SybaseInfoMaker and TOAD.
EnteroMedics, Roseville,MN. December 2008 – December 2011
Manager, DatabaseSystems.
Responsibilities:Develop and programclinical research databases usingClindex EDC with Sybase databasebackend.Clean
data to ensure data integrity and lock clinical research data usingtheSybase-based Clindex EDC system. Programdata
uploads fromexternal sources to MS SQL Server for the device database.Programstandard and ad hoc reports usingSybase
InfoMaker, MS SQL Reporting and Visual Studio.UsingExcel, InfoMaker and SAS, analyzeand trend data as appropriate.Using
SAS, combine data from various sources to provideto biostatistics.UsingInfoMaker and Word,create summary reports for
the Clinical Events Committee and Data Safety Boards.
Transoma, Roseville,MN. January 2008 – December 2008
Data Manager.
Responsibilities:Develop and programclinical research databases usingClindex with Sybasedatabasebackend.Clean data to
ensure data integrity and lock clinical research data usingtheSybase-based Clindex system. Program clinical research
standard and ad hoc reports usingSybaseInfoMaker.
Independent Consultant May 2005-January 2008
Responsibilities:Workingwith small medical device company to program databases in Clindex;and creation of clinical
research reports.

2. Marilyn Kaye Mowrey
2
Eminent Research / PPD Medical Device, New Hope, MN.
Director/AssociateDirector,Clinical Data Management. July 2002-May 2005
Responsibilities:Management of databasedesign analysts and SAS programmers. Development and implementation of
standard operatingprocedures and departmental processes.Directand manage project team specification meetings to
determine scopeand limitation.Providedepartmental and project budgets for resources,time and cost.
Clinical Data Manager. September 2001-July 2002
Responsibilities:Develop and programclinical research databases usingClindex with Sybasedatabasebackend.Program
standard and ad hoc reports usingClindex InfoMaker and TOAD. Train and supervisedatabasedesign analysts.
Clinical DatabaseDesign Analyst January 2001-September 2001
Responsibilities:Develop and programclinical research databases usingClindex with Sybasedatabasebackend.Program
standard and ad hoc reports usingClindex InfoMaker and TOAD.
St. Croix Medical
Clinical Research Associate/Data Management June 1999 - December 2000
Boston Scientific/SciMed March 1990 - May 1999
Clinical Research Coordinator
Executive AssistantClinical Research
Legal Secretary
Accomplishments
Autonomic Technologies:
Took on-linestatistical and biostatisticscourses to enhance analysisof data trending and combination of European clinical
data with U.S. clinical data.Programmed the EDC databaseusingClindex and wrote all necessary standard reports required
for trial management. Produced ad hoc reports as necessary.
EnteroMedics:
Created standardized reportingfor clinical devicedata,and assisted in creatingautomatic downloads of outsidedata into the
current MS SQL database.Learned basic SAS programmingto supplement statistical department in runningsimpleSAS
programs written in the biostatisticsdepartment.
Education
Kaplan University, Davenport, IA 2004-2008
Bachelor of Science in IT with databaseemphasis
Institute of Statistic 2013-2015
Biostatistics,statistical programming,data analysiscourses