I lead and oversee the delivery of critical study milestones across various scientific teams, ensuring projects are executed on time, within scope, and with the highest quality standards. My role involves strategic leadership of both direct and indirect reports, collaborating with external partners and consultants to drive scientific progress in bioanalytical, companion diagnostics, flow cytometry, and cell biology assays for both regulated (GLP, GCP, CLIA) and non-regulated studies.Key responsibilities include:Driving study timelines, budgets, and deliverables, while maintaining close communication with clients and senior leadership. Developing and implementing operational strategies to optimize processes, ensuring adherence to regulatory and quality standards. Managing cross-functional teams and ensuring alignment of project goals, resources, and budgets. Providing leadership in study management, ensuring continuous improvement of business processes, and acting as a key escalation point for client issues.With a focus on operational efficiency and project success, I aim to foster collaboration and ensure the timely execution of high-quality study deliverables.

Oversaw a team of 15-20 Principal Investigator level and analyst level individuals in support of PK and immunogenicity sample analysis and validations for BMS drug compounds (ADC, mAb, CAR-T, etc). Managed a team of 7 principal investigators supporting over 150-200 protocols of pharmacokinetic and immunogenicity assays in order to meet communicated timelines.Proactively managed life cycle maintenance of over 10 drug compounds and critical reagents to ensure zero downtime analysis for study timelines.Supported principal investigators in detailed review and assay troubleshooting of PK and immunogenicity analysis data to optimize performance and the ability to maintain high throughput analysis. Worked closely with protocol execution teams, clinical operations & external vendors to manage all operational activities required to deliver global clinical trial data.Demonstrated exceptional ability to prioritize timelines to meet all rapid turn-around and communicated deliverables.Exceptional detail oriented review of protocols, bioanalytical plans, result transfers, and study reports to ensure high quality written communications according to BMS best practices.Communicated directly with BMS stakeholders regarding timelines, assay trouble-shooting, and scheduling prioritizations.Trained principal investigators on day to day operations, methodology, analysis review, report review, and management of protocols.

Lead a team of 10-15 bench analysts in support of sample analysis for BMS protocols. Monthly, Quarterly and Yearly meetings with direct reports to disseminate company communications, maximize individual and team performance and foster morale to maximize performance. Weekly and monthly meetings with lab managers and other interdepartmental teams to ensure proper resource allocation to ensure coverage, accomplish client goals and meet client deliverables. Financial responsibility of contract review, modification and billing ensuring company fiscal goals were achieved.

Principal Investigator of over 50 protocols for GCP/GLP/Phase 1-IV studies ensuring shipment coordination, sample analysis, data review and data transfer to meet client expectations. Monthly and semi-weekly team and client meetings to ensure clients were informed of new and existing processes to ensure expectations. Leading team of 10-15 analysts in following latest FDA Guidelines and internal SOPs. General Supervisor that managed over 15 methods and team members to maintain communication with clients to achieve rapid turn-around of patient results. Ensuring continuing GLP, GCP and CLIA regulatory compliance with FDA, CDC, US Dept. of Health and Human Services, and Centers for Medicare and Medicaid to meet highest standards.

Day to day analytical lab work utilizing both quantitative and qualitative methods for pharmacokinetic, vaccine and antibody analysis in various matrices. Performed complex sample preparation, data reduction, troubleshooting and first level data review to meet client expectations. Increased competency and productivity through on the job training, adherence to SOPs, and independent learning. Trained junior analysts on day to day operations, reagent preparation and methodology. Team liaison for company vision of digitization of methods and notebooks.

· Used ArcGIS to create and edit shapefiles and analyze movement corridors · Created maps in GIS for publication in journal articles and other presentations· Extracted genomic DNA from plant and insect samples· Amplified microsatellite loci through the use of pcr· Resolved genotypes through agarose gel electrophoresis and capillary electrophoresis· Analyzed genotypic data with regression and other statistical techniques using the statistical software R· Published findings in scientific journals

· Taught molecular biology techniques and theory to senior level undergraduates, such as: Pipetting, DNA, RNA, and protein extraction, PCR amplification, gel and capillary electrophoresis, DNA cloning, and ELISA assays, Plasmid transformation using E. coli· Constructed and maintained PowerPoint and handouts· Generated tests and quizzes to evaluate student understanding of techniques and theories· Maintained and ordered laboratorymaterials· Managed laboratory budget