Support and Services
Office Hours with ClinicalTrials.gov Team
- Schedule an office hour at any stage of your project.
- 30-minute appointments at no cost.
Please review the list below to identify the best member to consult with you:
Jesse Reynolds , M.S., is a biostatistician at YCAS, he serves as the Director of the ClinicalTrials.gov Team at Yale University. Jesse has more than 10 years of experience working as an administrator in the ClinicalTrials.gov Protocol Registration and Results System (PRS). He specializes in determining registration and reporting requirements according to statute, as well as by funder and publication requirements. Results entry across various types of research and study designs is his area of expertise on the team.
Christina Barone , M.S. is a Research Assistant and PRS Administrator that specializes in clinical trial registration, PRS account management, troubleshooting, handling record errors, and study results entry. She is also a member of the national ClinicalTrials.gov Taskforce.
Sarah Andrychowski , MSHS, CCRP Currently, all interventional and observational studies/trials taking place within YCC need to be registered with CTRP because YCC is an NCI-Designated Cancer Center that receives a P30 grant. Sarah manages CTRP registrations and accrual reports for YCC. Reach out to Sarah for any questions or concerns, including but not limited to the topics below:
- Whether CTRP registration and accrual reporting is required for their study
- Information needed for trial registration and accrual reporting in CTRP
- Frequency of accrual reporting
- Accrual reporting for outside participating sites on multi-center trials
- Relationship between CTRP and ClinicalTrials.Gov
Schedule an office hours appointment here.
For Login Information or General Questions
Please contact our Yale team: yale.ctgov@yale.edu