Jeff Bock Email & Phone Number

Winston-Salem, NC, US

Morrisville, NC, US

Global head of technical delivery services across Clinical Data Sciences. Remit includes Clinical Programming (EDC, SAS, etc), Medical Coding, Randomization Services (IRT) and Clinical Data Analytics Services.

Morrisville, NC, US

Head of North American operations. Leading EDC and SAS development services. Also responsible for global IRT development and project management services.

Morrisville, NC, US

• Leading reporting, analytics and randomization services for global data operations. Responsible for strategic technology evaluation and implementation planning in support of functional areas including data analytics.
• Data visualization and analytics development.
• Global head for Randomization Services Group, providing consultation services and implementation of IRT solutions.
• Implementation of Centralized Statistical Analytics and analytics platform services.
• Development of Key Risk Indicator dashboard in support of centralized monitoring and RBM activities as part of ICH E6 R2.
• EDC and SAS programming services.

Durham, North Carolina, US

Durham, North Carolina, US

Head of Statistical Programming for a group of strategic and key accounts. Managing a team of programmers and managers responsible for all aspects of statistical programming deliverables, including input into statistical analysis plans, specifications for deliverables, SAS programming, standards management, macro development and creation of deliverables.

Durham, North Carolina, US

• Managing a group of 11 technical experts responsible for clinical database and statistical programming. Team responsibilities include:
• Implementation of eCRF screens and edit checks in multiple EDC systems, including InForm Architect and Central Designer. Creation of clinical study specifications; translating protocol requirements into implementation.
• Clinical data extraction programming (ETL) and SDTM delivery. Validation development using SAS/SQL/Cognos/etc. Data manipulation and aggregation/integration using SAS.
• Programming and technical support for processing clinical data from all sources: eCRFs, paper CRFs, ePRO and eDevice vendors, eHR data, labs etc. Spotfire delivery supporting data visualization and Risk-Based.

Brentford, Middlesex, GB

• Managed an international team of 13 specialists responsible for delivery of clinical data acquisition and provisioning systems. Group responsibilities include:
• Clinical study specifications; translating protocol requirements into implementation of a trial. InForm Architect & Central Designer eCRF screens and edit check development.
• Clinical data extraction programming (ETL) and SDTM delivery. Validation development using SAS/SQL/Cognos/etc. Programming and technical support for processing clinical data from all sources: eCRFs, paper CRFs, ePRO.
• Delivery of components for annual safety reporting (DSUR) and data collection components for regulatory submissions/applications. Computer systems validation adhering to 21 CFR part 11 requirements.Core.
• Managed group delivery of eCRF package for 53 studies achieving 98% on-time targets for study start.
• Implemented single provider CDISC SDTM Conversion Service for use by 120+ trials per year saving an average of 30% over cost of ad-hoc conversion efforts.

Brentford, Middlesex, GB

• Led end-to-end process redesign for eDM across study setup, data management and monitoring activities. Led the overall evaluation for the eDM Optimisation Project, a strategic initiative to replace the data management.
• Developed business case for new eDM implementation estimating peak OPEX and productivity benefits of £5.5M p.a.
• Directed 12 evaluation teams to successful creation and presentation of summary eDM recommendations.
• Delivered eDM evaluation methodology proposal to programme steering team receiving SVP endorsement from business and IT functional lines.

Brentford, Middlesex, GB

• Business System Owner for three applications related to the management and tracking of clinical data, laboratory samples and other external data. Ensured systems were maintained in a validated state in accordance with.
• Increased clinical scientist activity by 500% during Data Visibility pilot through targeted and individualized demos.
• Saved £11K by developing a novel approach for eLearning and User Guide integration, eliminating duplication.
• Led international team of 10 in testing a clinical data tracking system, completing validation testing in less than 4 weeks.
• Managed roll-out of a clinical tracking application to 60 study teams in 4 months, exceeding uptake targets by 50%.
• Saved 150 hours of UAT effort per year by developing a standardized testing procedure for recurring system upgrades.

Brentford, Middlesex, GB

• Responsible for implementation of processes and tools supporting multiple electronic Data Capture (eDC) systems. Provided technical leadership and support to a global network of eCRF programmers. Designed and developed.
• Developed data extraction using automated ETL scripting for internal RDC tool with DBMS/Copy and SAS, reducing setup time from 10 days to 2.
• Led development of a clinical reporting system providing real-time query listings, saving over 5,000 hours per year.
• Coordinated a rapid response team that delivered the validation rules for a study in 2 days, a 90% timeline reduction.

Brentford, Middlesex, GB

• Responsible for development of data capture packages for clinical studies, including Case Report Form design and programming of data cleaning checks. Developed therapeutic standards for CRFs and data cleaning checks to.
• Developed a clinical tracking and analytics application to predict subject visits and identify missing data.
• Created a study conduct dashboard to summarize data cleaning metrics for monitoring staff performance.
• Led Therapeutic Standards Team in defining and agreeing on TA standard validation checks.
• Experience in Oncology, Metabolic Pathways, Cardiovascular and Dermatology.

Master Of Science, Information Sciences

Bachelor Of Science, Computer Science