-- Responsible for providing operational support and expertise while interacting with and supporting internal matrix partners and external partners (e.g., GSK staff and vendors) across all VH Global Medical (GM) and Franchise Medical (FM).-- Line Manager responsible for developing and overseeing direct report(s) and leading matrix team members: o Coach, support, and develop direct reports, resulting in attainment of all performance plan goals. o Provide detailed, meaningful, and accurate feedback that includes fair performance evaluations.-- Provides detailed understanding of, and expertise with, source and tracking systems used by VH Operations -- Responsible for the accuracy and integrity of data within source and/or tracking systems through independent and proactive gathering, entry, and interpretation of information.-- Responsible for representing VH on appropriate working groups and proactively communicating with the Operations Team any updates and/or changes to the source systems software-- Coordinate and manage the operational activities related to internal committees, with responsibilities including, but not limited to, meeting planning, agenda development and meeting minutes.-- Identification, development and enhancement of study specific processes and procedures for operationalizing studies, while adhering to standardization and sharing of best practices. -- Review and track study invoices and accruals, including resolution of investigator grant payments, invoice accuracy, comparison to contract and outstanding payments and assist with Fair Market Value Assessments.-- Compile and analyze study budgets from Collaborating Partners to ensure consistencies-- Accountable for partnering with matrix partners to develop accurate milestone forecasts.-- Responsible for providing operational support for all Registrational Supported Collaborative Studies.-- Oversees the maintenance and archiving of electronic study files for ISR program.

-- Developed and led 6-month project archiving 10 years of backlogged studies covering all investigator-sponsored studies.-- Working with clinical, legal, financial and compliance directors to ensure FDA standards are upheld prior to final study archival.-- Assisting in the restructuring and implementation of ViiV's supported study management system.-- Restructured the file structure for ViiV's supported study management system.

--Head CTA on numerous studies including phase 1 breast cancer malignancies, (2x) phase 3 diabetes mellitus, phase 3b schizophrenia and phase 3 clinical depression.--Eagerly approaching new challenges and new studies in various indications as opportunities to diversify and increase clinical knowledge and experience. --Collected portfolio of managerial kudos, recommendations and highlights detailing work ethic, responsiveness, and efficiency.--Actively works to maintain healthy relationships with sites, sponsors, managers and coworkers through open communication and by actively seeking ways to assist.