Skill Set: Business analysis, change management, client relationships, data migration, disaster recovery, integrated learning support, project management, ELC / SDLC methodology and documentation, pharmacovigilance, portfolio management, quality assurance (including FCPA, HIPPA, ISO, Safe Harbor, SOX) / validation (EU / FDA, UAT), release management, requirement management, risk management, security, usability engineering, vendor management, workflow management System Expertise: Drug Safety, CAPA, clinical, CRM, DAM, dashboard, EDM, ERP, ETL, event tracking, infrastructure, MOM, MRM, SFA Professional Experience

May 2009–present: Confidential,NJ. . Role: Drug Safety PROJECT MANAGER.

Responsibilities: Manage ETL and DAM development, multidivisional vendor–executed data migration / integration and deliverables (data profiling, source-to-target. requirements, data architecture) from ARISj drug safety system, global proprietary drug safety system, and statistical reporting data warehouses into ARGUS; develop requisite ELC documentation; oversee validation, off-shore testers. and change management. Systems/Tools: ARISj, ARGUS, Documentum, Microsoft Project, Mercury Test Director, SharePoint. Trackwise, Visio

Jan. 2008–May 2009: Confidential,NJ. Role: SALES&MARKETING PROGRAM MANAGER / BUSINESS ANALYST.

Responsibilities: Partnered with solution architect and global users to determine solution; gathered green-field business requirements, developed business / functional requirements for Global Medical Affairs: medical-legal review / submission / reporting, expert engagement/grant payment systems and requisite infrastructure pending SAP ERP / Siebel MRM and SharePoint portal implementation and Global Sales & Marketing application; developed traceability matrix, test cases and summary (SDLC), conducted user-acceptance testing; oversaw change management.. Systems/Tools: Aprimo MRM, Cognos, Documentum, First Doc, Interwoven Team Site, JIRA, Microsoft Project, North-Plains Telescope, Protrack, Remedy, Siebel MRM/Pharma, SharePoint/, TIBCO Business Studio BPM, Visio

Jan. 2007–Jan. 2008: Confidential,NJ. Role: Drug Safety PROGRAM MANAGER/BUSINESS ANALYST/VALIDATION ENGINEER.

Responsibilities: Managed data migration and off-shore application development and enhancements to a proprietary global Web-based pharmacovigilance (drug safety reporting system (incorporating CIOMS / PSUR & EMEA) in a validated environment; worked with US and EMEA users to gather region-specific business/functional requirements; developed project plan/schedule, design specifications, use cases, release/test plans; test cases/ summary report; test enhancements; designed application Web pages and regulatory reports; reviewed validation qualifications and SOPs (SDLC); oversaw change-management process; worked closely with QA to ensure global compliance. Systems/Tools: Actuate, Documentum, Mercury Test Director, Microsoft Project, Remedy, Trackwise, Visio

May 2006–Dec. 2006: Confidential,NJ.Role: SALES&MARKETING PROGRAM MANAGER/BUSINESS ANALYST/VALIDATION ENGINEER.

Responsibilities: Managed off-site application and infrastructure development and enhancements to global clinical trials tracking system and Site Builder Web sites and G2 Single-Identity Remote Access portal (collaboration framework—Inform, Oracle, SQL. SharePoint, gathered green-field business requirements; developed project plan/schedule, use cases, functional requirements, design specifications, test plans, test cases, traceability matrix; prepared summary reports; developed global SOPs (SDLC); worked closely with QA to ensure global compliance. Systems/Tools: ClearQuest, Documentum, Inform, Interwoven Team Site, Mercury Test Director, Microsoft Project, Mime, SQL, Visio

Jan. 2005–May 2006: Confidential,NJ. Role: PROGRAM MANAGER/BUSINESS ANALYST/VALIDATION ENGINEER.

Responsibilities: Partnered with solution architect and global users to determine solution; drafted project plan/schedule, gathered best-of-breed business requirements, developed functional/design requirements for infrastructure supporting an SAP ERP implementation and remediation/integration involving 173 .Net/VB-Oracle/Lawson/Randstad/Controller Plus/AS400/MFGPRO/EDI/Galt/Sales Force Automation legacy applications and 279 data interfaces in a validated environment; developed use cases, test plan, test cases, test summary (SDLC) globalized training material; executed test cases; delivered instructor-led training; ensured ISO/Sarbanes-Oxley/EU compliance and change management procedures; worked closely with QA to ensure global compliance. Systems /Tools:SQL, Mercury Test Director, Mercury Test Director, Microsoft Project, TrackWise, Visio

July 2004-Jan. 2005: Confidential,NJ.Role: PROGRAM MANAGER/BUSINESS ANALYST/SOFTWARE QUALITY ASSURANCE for J.D. Edwards One World implementation.

Responsibilities: Drafted project plan/schedule, developed Sarbanes-Oxley/21 CFR Part 11/820 -compliant qualifications; reviewed test results, change requests, protocol results; developed use cases, policies/procedures/work instructions (SDLC) for J.D. Edwards One World with MES bolt-on (LDAP authentication) and MFGPRO ERPs, mainframe applications (including AS400), and infrastructure/middleware; worked closely with QA to ensure global compliance. Systems/Tools: QUMAS DocCompliance, TrackWise

Education: Ph.D. Romance