John Perryman Email and Phone Number

• Leading data management for clinical programs, ensuring high-quality execution within budget and time frames.• Innovating in data processes and systems to support clinical trials.

• Drove data management strategy, planning, and execution across multiple clinical programs.• Ensured all data management activities complied with regulatory standards.

• Managed vendor relationships and aligned data management functions with global program leaders.• Contributed to departmental staffing strategies and led cross-functional collaborations.

• Oversaw data management and technology strategies, leading a team towards successful clinical data integration.

• Provided leadership in data management programming, setting global development program standards.

Provides data management programming expertise and independent leadership for solution development at a therapeutic area level. Defines and implements the programming strategies and technologies to meet the requirements of global development programs. Ensures timely and reliable transfer of clinical study data from external sources to Takeda. Develops, manages and enforces standards and technologies for the collection, validation, coding and storage of clinical study data to maximize global data integration and inter-program efficiency. Directs the work of external vendors providing data management programming capabilities on complex therapeutic programs to achieve quality, timely, cost-effective study deliverables. Evaluates and leads new technology assessments related to clinical data programming and data management technology improvements.

Performs and manages tasks related to data quality and the implementation of clinical data standards specific to database build and analysis & reporting, within a program or group of programs, for Millennium outsourced studies

Design and develop electronic Case Report Forms (eCRFs) screens based on dataset specificationsDesign, develop and unit test eCRF check programming based on Data Validation Specifications using xml and VB Script programmingDevelop PL/SQL scripts to extract data for reports for Clinical Data Scientists and to assess quality of trial metadata prior to 'go-live'Troubleshoot Design and Build issues, propose resolution plans to GSK Programmer Analysts and implement changes when appropriateProvide technical guidance and support to achieve successful delivery of clinical studiesProvide training and mentoring for CDM staff and contribute to development of technical resource within therapy areasProvide consultancy to other groups outside the CDAD departmentAnalyse data capture problems/opportunities and develop and deliver high quality solutionsProgram source data mappings to SI datasets and troubleshoots data integration problemsWork with study team to ensure completion of all user acceptance and validation activitiesPropose and build programming standards across site, compounds, and therapy areas Act as a coach and mentor in area of expertiseContribute to the business requirements for the development of future toolsWork with Phase Forward's CAG department to investigate problems and devise solutionsAnalyse post 'go-live' changes, propose best method of implementation and advise study teams on the impact of the trial update

Build and test databases for the entry of data associated with clinical trials Create and maintain Clinical Data Warehouse metadataCreate design and mapping specifications for loading data into the Clinical Data WarehouseBuild and test programs to transfer/transform data from Biogen Idec's data entry systems (InForm, Clintrial and Oracle Clinical) or other sources into the Clinical Data WarehouseMonitor data transfers from external sources for data integrityDesign and develop PL/SQL data integrity checks Review the Data Review Guidelines and program Visual Basic Script edit checks as specified in Data Review GuidelinesDevelop Clinical Business Object reports for Clinical Data ManagersProgram ad-hoc listings using PL/SQLParticipate in development of departmental SOPs and guidelinesServe as a subject matter expert for InForm (Electronic Data Capture) and Oracle ClinicalServe as the Lead Clinical Programmer on the study management team.Create and support other applications in support of the departmentPerform validation of software applications

Design and develop eCRFs Program data mapping and extracts to a customer defined database schemaProgram data validation checks and rules specifications based on the eCRFsProgram rules for Phase Forward's InForm using XML coding and VB scriptingTrain sponsor and site personnel on InForm's use Assist the Technology Transfer department with rollout of software to clientsImprove trial development process and practice through innovative approachesResource and plan projectsAnalyze and improve work flow processesAuthor work instructions and provide input into SOPsCoordinate project specific workflowsProvide assistance and support to sales staff to attract and obtain new clientsServe as mentor for new employeesWork with the Products and Technology department to create new applications for InForm as well as enhance existing componentsServe as primary system design contact for clients

Clinical data validation and verificationTesting validation programsCoordinate project specific workflowsQuality control of clinical dataReview of data discrepancy listings with associated data query documentationAssisting and providing input into the development of Case Report FormsLiaising with Clinical Research Associates, Drug Safety Associates, Project Management and Database Management in clinical and technical issues