Allesia Tilton

• Lead clinical data management processes, including data validation, entry, curation and quality assurance for Early Phase I- Phase IV National Cancer Institute clinical trials
• Maintain database validation checks, ensuring data accuracy and protocol compliance.
• Perform QC audits and collaborate with research teams and respond to inquiries to resolve issues submitted via ServiceNow by the cancer research community or stakeholders, utilizing excellent communication and research skills
• Conduct UAT for new database applications, ensuring functionality and compliance with clinical trial regulations
• Train new data analysts and external personnel on clinical data procedures and software applications
• Develop and maintain training materials, external user guides, and project documentation, ensuring adherence to SOP and compliance standards

Key Achievements:

• Streamlined NCI clinical trial processing SOPs, reducing processing time by 50%
• Led the development of external user guides, ensuring consistent training and compliance adherence

• Led protocol and database design, maintenance, CRFs, and quality control efforts, ensuring compliance with GCP, ICH, and FDA regulations
• Directed all aspects of clinical trial operations including recruitment, informed consent, scheduling and performed clinical trial study visits, and research related interventions by following protocol regulations, HIPAA, GCP-ICH, IRB mandates, and clinical monitoring requirements
• Managed patient billing, insurance verification, and claims reconciliation for clinical trials
• Managed data entry, retrieval from Epic, and analysis, maintaining large datasets for clinical research studies
• Created, managed, and maintained large databases in the electronic data capturing system REDCap and ensured quality assurance and compliance with study protocols

Key Achievements:

• Served as lead clinical research coordinator for protocol development and study implementation, reducing start-up timelines by 15%
• Co-authored 10+ publications and abstracts, advancing knowledge in hematologic malignancies

• Assisted with study start-up processes, including IRB submissions and patient recruitment
• Performed data entry, quality control, and safety reporting, ensuring compliance with clinical and medical guidelines
• Managed and maintained large databases using REDCap, ensuring data integrity and protocol adherence