Eric Weise Email & Phone Number

Waltham, Massachusetts, United States

Collaborate closely with multiple Biotech and Pharmaceutical companies in the US and EU to provide Spotfire-based visual analytics solutions for reviewing and analyzing their clinical trial data.• Provide Business Analysis expertise, engaging with customer Study Teams to understand their business process needs, gather requirements, and deliver solutions that provide key analytical insights, promote better understanding of the data, and inform their clinical decision-making activities.• Serve as Tech Lead on multiple projects, guiding and supporting small teams of developers and platform experts to identify and deliver quality solutions using a fast-and-flexible approach. On smaller projects, act as both Tech Lead and Developer. Carry out Spotfire application and platform administrative tasks as needed.• Assist customer Study Teams with guidance and training on the usage and interpretation of the data visualizations.• Provide Subject Matter Expertise to customer Study Teams and internal teams regarding Best Practices for visual presentation and analysis of clinical trial data.

South San Francisco, California, Usa

Manage and provide support for Spotfire and other enterprise reporting tools across all functions in Product Development. Provide Systems Analysis expertise in support of Business Intelligence and Analytics initiatives, solutions and processes.• Serve as the Solution Lifecycle Manager for Spotfire, coordinating and participating in all lifecycle activities including the initial implementation of Spotfire for Product Development. Define and manage lifecycle activities, deliverables and timelines. Create and manage solution documentation as required. Develop and execute IT test cases and coordinate User Testing. Provide third- and fourth-level support for end-users and projects.• Collaborate closely with global Business and Informatics partners and stakeholders on multiple projects to assess, define, develop, implement and support visualization and analytics solutions, with an emphasis on Spotfire.• Collaborate closely with internal Operational Support colleagues for incident and problem resolution and change management activities.• Serve as the Solution Lifecycle Manager for J-Review and Hyperion Performance Suite. Provide first, second and third-level support for these applications as necessary, coordinating and participating in all aspects of the system lifecycle. Provide third-level support for these applications.• Liase with vendors and other providers as needed.• Initiate, manage and execute changes (including decommissionings) for a variety of systems and integrations.• Ensure adherence to established system and project lifecycle processes.

South San Francisco, California, Usa

Perform Business Systems Analysis, Change Management, Software Quality Assurance and System Support activities as required, for a variety of systems supporting clinical trials for Product Development.• Collaborate with colleagues from multiple functions to assess needs and requirements, and identify potential solutions.• Perform SQA activities for a variety of custom integrations to the RAVE electronic data capture system, including development and management of related documentation, creation and execution of test cases and supporting SQL scripts, and defect analysis/resolution.• Initiate, manage and execute changes (including decommissionings) for a variety of systems and integrations.• Ensure adherence to established system and project lifecycle processes.• Review and execute System and Integration test cases for the Global Integrated Drug Development Environment (GLIDE).• Review clinical trial definition specifications and configure RAVE integrations accordingly.

San Francisco Bay Area

Manage the lifecycle of, and provide user support for, major enterprise reporting tools. Perform requirements-gathering, evaluation, testing, documentation, implementation and maintenance activities for applications and processes used in the conduct and analysis of clinical trials, with an emphasis on reporting tools. Lead global teams comprised of both Informatics and Business colleagues in support of these tools.• Serve as the primary Solution Lifecycle Manager for Hyperion Performance Suite, Report Launch Pad and the Patient Summary System, coordinating and participating in all system lifecycle activities. Lead global teams responsible for supporting these applications. Provide first- through third-level support for these applications.• Serve as a Solution Lifecycle Manager for Oracle Clinical, Integrated Review, and other related applications, assisting in all aspects of the system lifecycle. Provide first- through third-level support for these applications.• Ensure adherence to established system and project lifecycle processes, including CSV, ITIL and IPMPF.• Provide subject matter expertise in all areas of clinical trial data reporting.• Collaborate with colleagues from multiple functions to assess needs and requirements, and identify potential solutions.

Provide expertise in the analysis, selection, usage, training and further development of tools and applications used in the reporting of clinical trial data. Interact with Informatics and Business colleagues to provide support for, and collect feedback on, reporting tools and applications. Use extensive knowledge of technical and business processes to provide useful and efficient tools to meet clinical data review requirements in the Roche environment.• Serve as the global Informatics development expert for Brio Query and related applications in the Brio Intelligence suite, developing technical solutions and providing support for query/report developers and end-users.• Serve as the global application manager for the Patient Summary System. Interact with end-users and application developer to provide application support and troubleshooting. Coordinate ongoing development of the tool, and develop/maintain application lifecycle documentation. • Collect, evaluate, prioritize and implement requirements, requests for bug fixes, and/or enhancements for new and existing applications in the area of clinical data reporting, including externally-developed tools such as Integrated Review. • Develop, maintain and/or execute Test Plans and Test Scripts for Informatics applications in accordance with standard processes and practices. Coordinate global testing activities, including the evaluation of test results and tracking/resolution of any issues raised.• Interact with Informatics and Business personnel to ensure that reporting needs are continually met

As the Roche Pharma Development Brio Query expert, provide direct and indirect support for the production and maintenance of clinical trial data reports in a web-enabled enterprise reporting environment. Apply knowledge of Oracle Clinical and other applications in conjunction with understanding of study conduct best practices to provide meaningful reports for Data Management, Clinical Operations, Clinical Science, Corporate Planning and other groups.• Provide Brio support for both local and global personnel as a member of the Roche Brio Global Support Team. • Interact with study team members and other individuals to develop solutions for their reporting requirements, including needs assessment, coding, validation and implementation. • Develop and maintain Brio training materials, including user manuals and online tutorials. Conduct training courses for both in-house and field personnel.• Maintain Brio Enterprise Server and associated Intranet web pages to ensure that study teams have ready access to current data.• Independently and in conjunction with end-users, identify and develop solutions for shortcomings in local and global data-review processes. • Serve as Global Component Representative for several aspects of Roche's Oracle Clinical database environment, including reporting tools and database security. Responsibilities include end-user support, troubleshooting, upgrade testing, and gathering of user requirements for enhancement requests.• Provide input and expertise for a wide range of Roche Clinical Systems initiatives, such as Remote Data Entry, Clinical Data Warehouse, and the GISMO Study Monitoring Tool.• Develop, implement, and/or execute test plans and test scripts for software upgrades.

An integral member of the Study Management Team responsible for international clinical trials. Performed Data Management functions during all study phases to prepare trial data for analysis.• Perform primary data management activities for 7 simultaneous international Phase III trials of various size and complexity.• Interact with Clinical Research Organizations to ensure timely collection of trial data and discrepancy resolution. • Interact with related internal functions to ensure timely case report form development, database setup, validation specification creation, data cleaning and ad-hoc report creation in order to provide a clean database for interim and final analysis• Provided data management input into the development of study protocols and amendments.• Assisted in database migration activities to convert a large Phase III trial from the existing IDMS database to Rx/Clinical (the predecessor to Oracle Clinical).

Chemical Engineering

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Computer Programming

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Education record