• Provide strategic direction and leadership to the Design PM team, overseeing planning, execution, and delivery of clinical technology projects.• Allocate resources effectively across multiple projects and programs, establishing performance metrics and evaluating Project Manager performance. • Foster a culture of learning and professional growth within the team.

- Client dedicated System Design PM.- Consult across functional teams/areas to streamline client standards for build and maintenance of IRT studies and related integrations.- Assist with retrospective reviews of study builds to decrease defects and subsequent downstream impacts to quality.- Constantly explore automation capabilities to increase cross-functional team productivity.

Build and maintain IRT/ECOA systems for pharmaceutical clientsResponsibilities include:• Assess client’s needs and provide innovative solutions to optimize their study and/or program• Resupply optimization • Risk assessment/mitigation• Client program management & Optimization• Consult with cross-functional teams to initiate client-driven enhancements• Study design review and identify downstream impacts• Coordinate programming & customizations tailored to the client’s specific requirements• Strategic account management focused on the IRT aspect • Coordinate randomization design• Follow agile fundamentals • Consult clients of various scales with their IRT design and implementation to align with their protocol• Collaborate with a cross-functional team to ensure project timelines are met.• Guide the client through the IRT setup process to ensure it maximizes their trial capabilities.

• Collaborated with internal clinical study teams, as well as Bio-delivery & Statistics, Logistics, and IT to initiate, maintain, and close out studies. Responsibilities included:• IRT configuration analysis • IP Management and forecasting• Validation plan creation & execution • Internal & external training• System configuration & testing • GxP compliance monitoring• Study requirements definitions • eTMF updates/contributions• Implemented agile principles to optimize team productivity and on-time project deliverables. • Assisted with legacy IVRS studies, including data management and logistical forecasting.• Ensured that IP releases occur as planned and prevent disruption of upcoming patient dispensing visits.

• Consulted clients during the requirements gathering phase to optimize the IRT to fit their protocol needs.• Maintained all study documentation for study start-up, implementation, maintenance and close-out of the project. • Participated in investigator meetings to conduct training and explain the IWRS capabilities.

Associate Project Manager/Associate Business Analyst with experience in the following therapeutic areas:Ophthalmology, Oncology, Infectious Disease, Cardiovascular, Respiratory• Supported more than 12 Phase II and III clinical studies simultaneously.• Interacted with clients to gather requirements for mid-study updates.• Managed inventory releases for study start-up and maintenance. • Identified and recommended modifications to existing study designs and processes to better meet client needs.

• Assisted clinical sites and sponsors with phases I-III of the clinical trial. • Partnered with Project Managers to improve and rectify drug supply issues directly with sites and sponsors.• Safeguarded the staff from entering information into the EDC and IWRS that can un-blind staff and compromise the study.• Maintained user permissions in various Imaging/eClinical products to match the appropriate role.• Performed troubleshooting steps for site issues that can delay the study or increase costs for the sponsor and site.• Gained imaging data entry experience in multiple therapeutic areas including CNS, Oncology and MSK.• Assisted clients around the world with many data entry, IWRS/IVR and Imaging queries.

Assisted the Director of Marketing with creating material for local blood drives.Created and edited copy in multiple forms.Ensured that deliverables were on-time and accurate.