Provided line management and leadership for analytics projects and analysts to improve Early Clinical Development (ECD) support and cross-functional collaboration.- Engaged stakeholders at various levels across ECD to answer questions, resolve challenges, and continuously evolve the group's methods to provide support and improve operational efficiency.- Oversaw personnel and project-focused efforts of up to six analysts (contractor and FTE).- Worked with the predictive analytics lead to define, develop, and assign Genentech Predictive Analytics (gPA) team goals and projects supporting clinical operations in ECD.- Collaborated cross functionally with other analytics groups across Roche to increase engagement and streamline offerings to ECD. This ensured consistent analytics and universal understanding of data challenges that were being evaluated.- Worked with the Health Equity and Diversity and Inclusion groups within Roche to evaluate and select sites for alliance relationships. This resulted in an overall increase in enrollment in target populations wherever these alliance sites were engaged compared to the overall average for the same studies.- Created data visualizations and dashboards to encourage self service with curated data. This decreased lead time when clinical operations sought quick answers and ultimately sped up the overall decision making for trials and portfolio analyses.

Acted as analyst, managing individual projects and deliverables. Also acted as interim Analytics Lead from 2019 through 2021 for gPA team, managing personnel in gPA and team goals.- Led (and supervised) up to eight analysts, helping them effectively engage with clinical operations study teams and identify areas for personal and professional development.- Oversaw resourcing and project adoption and management of contractor, consultant, and FTE positions for ECD’s Predictive Analytics (gPA) group from 06/2019 - 05/2021.- Defined, developed and assigned gPA team goals and projects to support ECD and increase data driven decision making.- Provided analytical support through core offerings to clinical operations, quality and compliance, clinical science, and leadership.- Collaborated on Manager’s Circle and Career Development sub-teams to improve career engagement and management skills for employees in ECD.- Created data visualizations and dashboards in support of the Cancer Immunotherapy Centre’s of Research Excellence alliance group at Genentech. This allowed for real time tracking of alliance sites and an increase in timely responses when performance concerns arose.

Provided data analytics to Clinical Operations and Resourcing groups through projects, study support and dashboard builds for self service.- Supported clinical study teams using historic enrollment information to help guide country and site selection and define enrollment timelines.- Managed resourcing and clinical operations support of all contracted analysts in gPA from 06/2016 on.- Developed biannual Partner Book of Business presentation to inform affiliates and partners of portfolio activity.- Worked with Cancer Immunotherapy group to identify 25 alliance sites for continual evaluation and engagement. This led to increased engagement and performance with these sites in a critical therapeutic area for Genentech.

Supported clinical study teams by using historic enrollment information to help guide country and site selection and predict enrollment timelines. Acted as analytics support and liaison for the resourcing group to allow oversight of how time was being spent in ECD.- Utilized TIBCO Spotfire data visualization software for various purposes, including developing a functional dashboard for the Resource Management Group.- Provided ad-hoc support to ECD clinical operations by analyzing and organizing CTMS data.

Split time between supporting the ECD Resource Management Group and gPA. Provided analytics that allowed the proper resource evaluations of the personnel in clinical operations while also providing study timeline projections to ECD.- Used Plansource and Excel tracking systems to help manage resourcing allocations for ECD clinical operations.- Helped inform study planning by leveraging historical clinical operations data to perform enrollment projections.

Created cleaning validation protocols and procedures. Executed equipment cleaning validation protocols to align with FDA requirements.- Developed protocols for executing cleaning studies and wrote reports to establish a potentially viable cleaning program for new products.- Oversaw cleaning validation process to ensure proper Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).

Created cleaning and process validation protocols and procedures. Executed equipment cleaning and process validation protocols to align with company standards and FDA recommendations.- Optimized cleaning procedures for validation and long-term implementation at the manufacturing plant.- Developed protocols for the execution of cleaning validations and wrote validation reports to establish a potentially viable cleaning validation program for the company.

Worked as summer intern, focusing on regulatory complaint handling and reporting for marketed Cochlear Implants.- Worked daily with Netregulus and DataFlo databases to create and search patient complaint records.- Responded to an average of 40 complaints daily. Determined which reports were complaints and which complaints were reportable.- Completed MedWatch form 3500A for all incoming reportable complaints throughout the summer.

Supervisor at 4 different locations around Northern California while attending undergraduate school.- Created daily and long-term goals for employees and implemented tracking systems- Led a team of approximately 20 employees