Tyler Becker

Job duties include:

• Clinical Trial Study Start-up, have brought 10+ studies to site activation.
• Preparation of IRB submissions, both locally and centrally.
• Creation and maintenance of Regulatory Investigator trial binders
• Training in GCP and ICH guidelines for Clinical Trials
• Creation and maintenance of source document builds in Redcap
• Collection and distribution of Safety Reports for Principal Investigator oversight
• Reporting deviations and adverse events to the necessary authority
• Led efforts to implement best practices in data management, ensuring accuracy and accessibility of critical records for internal review or external inspection purposes.

• Researched methods of cryopreservation and organ banking for transplantation
• Involved in experiment planning and execution, while following FDA regulations
• Involved in preparing grant submissions and reports to the NIH and DOD