Thomas Wilson

Thomas Wilson is an Oncology Clinical Research Consultant with a breadth of experience in various aspects of clinical research operations, data management, monitoring, regulatory compliance, drug and lab supply logistics, as well as CRO and vendor management including budget negotiations.

His expertise spans across different fields including biology (general, molecular, developmental), behavioral health, public health, and clinical chemistry with a focus on lab procedures and reference ranges.

Specializing in oncology clinical trials, Thomas has acquired in-depth knowledge of trial and protocol designs tailored to specific molecules, start-up procedures, budgeting expectations from participating institutions, and statistical analysis.

With a strong background in data and database management, Thomas has collaborated in laboratory research settings and multidisciplinary healthcare teams, actively participating in data cleaning, safety reviews, and co-authoring multiple published studies.

He holds certifications in JReview, completed training in ICH-GCP guidelines and 21 CFR part 50 via CITI courses, and upholds a data-driven approach to his work.

Thomas has a diverse professional background, having worked for sponsor companies, CROs, as a consultant, directly with patients, and in hospital and research settings.

His continuous focus on project management skills development has enabled him to support various biotech companies, and he remains dedicated to furthering his contributions and knowledge in the field.