Taylor Marshall Email & Phone Number

Seattle, Washington, United States

Direct report responsibility for Clinical Programmers (e.g., performance management, guidanceand mentoring) Project level coordination and day to day oversight of Clinical Programming tasks in the studylifecycle and estimating resourcing needs Manage CP deliverables in coordination with internal and external cross functional teams Align with the Data Management Leadership Team on creating efficient ways of workingDevelop process improvements which will be utilized within the clinical programming groupStrategize on innovative ways of working in areas such as EDC Build within clinical programmingProject level technical oversight of all Clinical Programming needsProvide programming expertise for external data management, database set up, CRF design,and data cleaning to efficiently ensure high quality dataCollaborate with Standards and SDTM Programming in development and design of operationalMetadata for all data received (external and clinical database)Responsibility for development of review output to support Data Management data reviewactivitiesOversee the creation and implementation of edit check specifications for EDC BuildOversee all external data importing, reconciliation programming, and identification of issuesthat may arise with external dataManage any additional Clinical Programming ad hoc requestsProvide guidance to study teams and external vendors regarding the technical aspects of clinicaldatabase structure and programmingServe as the clinical programming representative on cross functional teamsRepresent clinical programming activities for regulatory audits

Seattle, Washington, United States

Leading the development/implementation of the global library strategy and structures.Leading the global library team who create/update the global library.Leading the EDC system implementation to ensure adherence to best practices.Leading initiatives with broad, cross-functional impact (including strategic process and technology improvements), influencing direction and driving to completion.Contributing to the development and application of smart systems/tools and optimal approaches to support the collection of data with a standardized approach.Authoring procedural documents (SOPs, work instructions, job aids) and coordinating reviews/approvals. Developing and conducting training and/or mentoring team members on key activities and processes.

Seattle, Washington, United States

Ensure the EDC system is being developed and managed at a global level for effective use for study databases. Developed, implemented, and managde the global library strategy and structures. Lead in the build, maintenance, and review of the Medidata Rave global library standard objects Authored ,updated and reviewed procedural documents Developed and conducted training and/or mentored team members on key activities and processes.Liaised with and reviewed work delivered by external partners.

Greater Seattle Area

Oversee and lead development/creation of operational metadata and clinical databasesLead the development of external data transfer specificationssLead the development and maintenance of data review listings in SAS Provide oversight of CRO/vendor programming activities to ensure adherence of standards as well as receiving quality and timely deliverablesLead/Participate in study/project/programming meetings as a core member and provide technical expertise/supportAuthor, review, approve and train on department procedures including SOPs, Working Practices and Guidance Documents

Greater Seattle Area

Perform data management programming for various clinical trials as well as extramural partner trials.Maintain in-house trials which could include (develop programming, testing and maintaining clinical trial databases) in accordance with Celgene standards Develop, program, and test data review listings in SAS for data review purposesDevelop, program, test and maintain validation/edit checks in Medidata Rave Participate in and lead team meetings with cross functional team members.Liaise and oversee with CRO/vendors providers, when necessary, to ensure that Celgene standards and design are implemented in all studies

Greater Seattle Area

Perform data management programming for various clinical trials as well as extramural partner trials.Support all platforms and integrationsManage electronic data collection and access, all in accordance with GCP and Juno SOPs

Greater Seattle Area

Serve as interim director as neededRepresent Data Analytics department inside (and outside, but mostly inside) DF/Net as neededLead the development and maintenance of statistical programming standards and conventionsConduct code review on a regular basis to ensure that standards and conventions are followedWork with the director of department to write and maintain department SOPsSupervise statistical programming workflow – in particular, be responsible for workload distributionParticipate in performance evaluations Collaborate with director in recruitment of future department employees, including conducting phone interviews of statistical programmers

Seattle, Wa

Responsible for using statistical software packages to produce tables, listings, and figures in various outputs and specifications. Assist and/or write internal data checks to ensure data integrity. Work with the study Biostatistician on more complex statistical tasks such as the generation of SAPs and the conduction of study analyses. Tasks include:Manage and maintain operational reporting suites within the Data Analytics Department.Manage all lab data from third party vendors across DF/Net, including initial setup and commutations, programming, integrating, and reconciling lab data against clinical database.Supervise all data analytics staff associated with data integration and reconciliation from third party vendors.Represent Data Analytics department in company-wide initiatives.Negotiate pricing for select data analytics services and projects.Provide training and mentorship for incoming employees.Communicate daily with clients concerning analytic needs.Member of the Data Analytics hiring team.Advocate for continuing education program within Data Analytics.Program/validate analysis data sets and tables/listings/figures.Develop and test operational reports as requested by sponsors.Shell/Perl Scripting (program, test, develop scripts to run study reports as well as ad hoc programs). Provide programmatic support for various study needs (DSMB, Data Lock, Data Exports).

Greater Seattle Area

Created ad hoc operational reports.Integrated data into clinical databases from third party vendors.Created data cleaning edit checks, reports, and tables based on Database Manager or sponsor requests.Served as edit check subject matter expert and trained employees at DF/Net and client organizations.Supported Data Analytics department during periods of high workload.

Df/Net Research, Inc