Thomas Verish Email & Phone Number

Doylestown, Pa, Us

Alameda, California, Us

Provide leadership to the Clinical Data Operations & Strategy group to ensure the high quality delivery of trial and program-level data to support Early Development through Late-stage Development. In partnership with internal stakeholders, define and deliver the end-to-end data flows, including the necessary technologies, processes, and people to support the operations.

Boston, Massachusetts, Us

Provide the overall strategy and leadership for the functions of Data Management, Centralized Data Monitoring, and Data Standards and Integration. Key aspects of the position include:Leads the clinical data management organization to deliver data and strategic data science approaches that help expedite business decisions to strengthen the company's competitive edge delivered on a strategy to streamline data flow and support the technology platforms across clinical development. Building the Centralized Monitoring capability, including the enterprise level Risk-Based Monitoring (RBM) methodology and execution, to ensure compliance to clinical, protocol and regulatory requirements that help de-risking the clinical studies through identification and mitigation of site and data quality issues. Leading the planning for CluePoints platform implementation in 2023.Partnering with business and key collaborators to evaluate and implement the tools and processes necessary to aggressively drive our data needs in support of the organization’s drug development process. Implementing the eClinical Solutions Clinical Data Repository, as the ‘Clinical Data Management Workbench’ to transform how EMD manages clinical data.

Melbourne, Victoria, Au

Provide the overall strategy and leadership for the functions of Data Management, Clinical Programming, eClinical Operations, Central Monitoring, and Performance Improvement.Responsible for the development and maintenance of the overall eClinical and data strategies to support CSL Behring’s Clinical Development and TA strategies in compliance with industry regulations and best practices. Contributes to drug development plans, submission and life-cycle management strategies for all stages of clinical development. Driving a strategy that takes into account a focus on building an industry leading organization to support the investigator sites and patients.

Melbourne, Victoria, Au

Responsible for leading study execution and site monitoring for all therapeutic areas globally. Managed key CRO partnerships and internal team across North America, Europe, Australia and Japan to deliver clinical trials in rare diseases. Primary areas of responsibilities include Study Management, Site Monitoring, and CRO management

Melbourne, Victoria, Au

Provide the overall strategy and leadership for the functions of Data Management, Clinical Programming, eClinical Technology, Procedural Documents & Standards, and Operational Excellence. Key aspects of the position include:Responsible for the overall strategy and operational data management across all clinical programs. Process improvement underway to develop a guideline document on how DataOps will operate with internal and external stakeholders.Direct the entire data flow of clinical programs and studies to enable high-quality consistent and integrated datasets for regulatory submissions.Responsible to develop and manage the outsourcing strategy for CROs and technology providers. Acted as Interim Head of Clinical Development Operations.

Lawrence Township, Nj, Us

Responsible for the functional groups within Data Operations that provide services and support activities to the drug project teams. In particular this includes operational ownership of various applications and system-based capabilities including Oracle Clinical, Oracle Siebel CTMS, TMF, MyTrials investigator portal, ePRO, data integration and analytics.

New York, New York, Us

Responsible for global leadership and departmental management of the Global Clinical Data Services (GCDS) and Clinical Programming and Writing (CPW) organizations. Group is accountable to deliver quality centralized data management, programming and clinical study reporting services to all global sites for all studies run by Pfizer. Responsible for predicting and providing resources to support and enable drug projects to meet timelines in line with project priority and performance goals. Group consists of 230 Pfizer staff and 1600 external contractors. Dotted line management of 140 colleagues in Shanghai, China and Tokyo, Japan.

New York, New York, Us

6/2009 - 7/2011 – VP, Worldwide Head of Clinical Programming & Writing (Interim).4/2007 - 6/2009 – Sr. Director, Head, Clinical Programming & Writing Oncology Business Unit.10/2005 - 4/2007 – Sr. Director, Connecticut Site Head, Clinical Programming & Writing.9/2003 - 10/2005 - Director, Operations Head, Clinical Study & Data Management.3/2001 - 9/2003 - Associate Director, Operations Head, Data Management.9/1999 - 3/2001 - Manager, Data Management Therapeutic Group Leader.12/1998 - 9/1999 - Regulatory Affairs Associate.10/1996 - 12/1998 - Biometrics Safety Data Manager.

Washington, Dc, Us

Ms, Systems Management (Business)

Bs, Human Resource Management