We require 3 months minimum advance notice of services requested as well as a pre-Grant Proposal Submission Study Consultation
Support for Every Stage of Research
Proof of Concept Research
Working with new device concepts
Helping PIs develop novel applications of existing technology
Device troubleshooting and standardization of data collection
Pre-Funded Study Development
Consultation with the Clinical Research team during Weil Institute team grant proposal and project development for feasibility, budgets and pre-game troubleshooting from a premier boots-on-the-ground team
Mentoring, networking and templates for IRB applications and protocol development are available
Funded Research
Implementation and execution of research projects with internal or external funding
Study maintenance for IRB-approved applications
Data management and milestone reports
How We Help
Our team has provided essential assistance for investigators to secure over $10 million in federal and industry funding. Creating and testing innovative technologies with Weil has led to new patents, technology licenses, and the forming of new companies.
Leveraging adaptive design methodologies and the unique capabilities of an academic medical center,
the Clinical Research team has the right staff and resources to conduct a variety of studies.
IRB Management
Our team is skilled in managing IRB protocols and ensuring studies are compliant.
Application and consent form review
IRB compliance
Amendment submissions
Study Management
In addition to ensuring feasibility, the Clinical Research team will optimize the execution and
management of each study, including:
Obtaining access to vital data and patient records
Creating budgets
Providing frequent communication with the Principal Investigator
Screening and recruitment of patients
Obtaining informed consent
Sample and data collection
Pulling medical record information
De-Identifying protected information
Securely storing data and patient records
Entering study information into databases
Presenting data to key stakeholders
To learn more about our team and how we can help your research, click the image above to download an informational flyer (PDF)
Helpful Resources
IRB Protocol Development TemplatesInformed Consent Templates
Updating IRB Team Members
"The Clinical Research team has been invaluable in helping us conduct clinical research in the ICU. It is great to have access to these skilled and capable personnel to focus on important tasks like subject enrollment and research procedures."
Venkatakrishna Rajajee , MD, MBBS; Neurological Surgery, Neurology