Marilyn Kaye Mowrey Resume 2016
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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
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Marilyn Kaye Mowrey Resume 2016
- 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