Available Resources
We’ve been working hard to put together Resources that will help Penn Research Personnel conduct the day-to-day tasks required in clinical trials, and in hopes of preventing people from re-inventing the wheel. Enter your information to receive a copy of any of the available resources. Please note that not all resources are kept up-to-date and we welcome feedback/updates.
Recruitment Strategies Manual
Process Notes (detailed description of a Penn process including purpose, intended audience, description, key contacts & flow diagram)
- Archiving at Penn
- BAA & Information Security Review
- Certified Copy of Medical Records
- CHOP Credentialing
- CDA
- CTMS
- Penn Global Medicine - International Research Subjects
- Greenphire ClinCard
- Interpreter Services
- Penn IRB Reliance Agreement Requirements
- Non-English Speakers Using Short Form
- NucMed Ops
- Scheduling Ultrasounds for Research Studies
- Submitting a PDS Report Request
Checklists
- Site Assessment Visit Checklist
- Onboarding Staff to Active Study Checklist
- Study Closeout Checklist
- New Employee Start-Up Checklist
Trackers
- Study Start-Up Tracker
- CV, ML, Trainings
- IRB Reliance (things to document & tracker after agreement made)
- Feasibility Assessments
Miscellaneous resources
- Rating Labs & Procedures for Clinical Significance
- How to Draw a Pedigree
- Genetic Testing and IDE Determination
What resources would you like to see us develop? Are you willing to develop a resource for the DOM CTU?
Submit a request or sign up to develop a resource by completing the Resource Topics form and sending to the CTU.