• Spearhead collaboration with executive leadership across Clinical, Operations, and IT divisions to craft high-impact proposals for clinical trial services. • Expertly manage and refine comprehensive budgets and texts for key business documents, including RFIs, RFPs, and Work Orders. • Lead the proposal development lifecycle, ensuring excellence in consistency, quality, and adherence to strict timelines. • Demonstrate exceptional organizational acumen, balancing multiple high-stake projects and engaging various stakeholder groups. • Provide pivotal updates and insights on proposal progression, maintaining transparency and alignment with organizational goals. • Proactively mitigate risks to project timelines, ensuring smooth and efficient workflow. • Oversee CRM system updates, enhancing data accuracy and process efficiency. • Translate complex proposals and budgets into clear, actionable Work Orders and Change Orders. • Implement stringent quality control measures on all documentation, upholding high standards of accuracy and professionalism. • Maintain and evolve proposal and budget templates, ensuring up-to-date practices and adherence to industry standards. • Actively contribute to the evolution of proposal development procedures, collaborating with executive leadership for continuous process enhancement.

• Expertly manage the production and distribution of clinical outcome assessments for global sites, exemplifying leadership in navigating complex clinical environments. • Serve as the lead for scale management in CNS and pediatric rare disease trials, demonstrating specialized expertise and leadership in critical therapeutic areas. • Oversee the procurement and logistics of scale materials, managing a substantial budget of over $2M, showcasing adept financial oversight and operational acumen. • Take a pivotal role in the creation of RFPs and the provision of budgetary inputs for change orders, blending strategic planning with collaborative execution. • Collaborate effectively with sponsors, operational teams, and logistics providers to ensure site readiness for SIV, reflecting strong cross-functional leadership skills. • Provide mentorship and training to junior staff, fostering a team culture of continuous learning and professional development. • Manage vendor relationships, monitor purchases, and maintain a current database of vendor information, ensuring high-quality standards in clinical outcome assessments. • Perform key rater-training functions, including RES/REQ reviews and training deployments, highlighting a leadership role in maintaining training quality and standards. • Actively contribute to the development and improvement of training and learning management systems for studies, underscoring a commitment to excellence in clinical research.

• Create and maintain scales databases and libraries and project tracking tools• Oversees production of study specific source documents and secures licensing permissions• Leads projects for scale consultation and translations for clinical research studies on neurological and rare pediatric disease• Proposal and project development support• Manages a propriety ePRO database for studies for remote or electronic administration• Use of agile technologies for reporting and tracking • Manages logistics and distribution of scale materials for sites and raters

*Monitored the circulation and archival of controlled documents in compliance with GMP and ISO.*Created and reviewed logbooks, SOPs, Change Controls, and Batch Records for generic drug and would recovery medical device*Led and assisted internal audits**Site closed down in February 2018

*Perform quality assurance review to ensure compliance of reports for Bayer CropScience*Ensure EPA readiness through GLP requirements in both US and Canada studies *Attend trainings throughout RTP area and US regarding GLP compliance*Highly organized, detail oriented and able to handle multiple priorities and projects at one time

*Reviewed technical quality of scientific data with a consistently low turn around time and high output. *Collaborated with data reviewers to perform a statistical analysis of data that had been collected for 6 months to determine turn around time based on quality of reports. A metric was created to illustrate the cost impact of low quality reports and was used as training for laboratory departments.*Customer focused by establishing and maintaining Service Level Agreements.*Managed forecasting spreadsheet to present upcoming weekly projects and revenue to project directors*Audited department for compliance with 5S and cGMP*Served as a meeting scheduler and organizer for Catalent Women’s Network.

•Produced the Varivax vaccine using SOPs and cGMP•Operated in clean room environment to filter harvested viral fluids into clarified bulk •Proficient in the use of large thaw baths, skids, -70˚C freezers, and WFI stations, pumps, tube welders, filter testers, and sonicators•Managed SOPs for document control to ensure compliance in operations•Responsible for training other technicians in operation of equipment and procedures in PSF•Contributed and implemented process improvement projects•Performed review of Electronic Logbook and process

•Assisted in teaching and preparing lab materials for an introductory biochemistry lab under Dr. Trino•Managed chemical stockroom and preparation of chemical reagents, media, and experiments•Performed protein assays, chromatography, spectroscopy, electrophoresis, and data analysis•Maintained proper lab protocol in classroom

•Investigated plant pathogen, Ralstonia solanacearum, under the supervision of Dr. Mila in Plant Pathology •Performed bacterial assays, CFU analysis, media preparation, and other microbiological techniques •Experience in greenhouse techniques•Created and presented poster of research at NCSU Undergraduate Research Symposium

•Taught and facilitated lab activities to 18 undergraduate students under Dr. Mickle•Taught and set up lab exercises such as dissections and electrophoresis and maintained proper lab protocol