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Interested in learning how to be more creative about patient recruitment strategies?
What can we learn from medical conditions experienced by both humans and animals?
How do you assess the feasibility of your study's recruitment plan?
This program is also a good refresher for experienced PIs. Topics covered include regulatory processes, stakeholder and community engagement, participant recruitment, adverse event reporting, audit readiness, and study close-out.
How can data help us to better understand and respond to the synchronization of infectious outbreaks?
How can data help us to better understand and respond to the opioid crisis?
What makes a successful grant proposal?
How do you strategically build a strong grant proposal team?
What is comparative effectiveness research (CER), and why is it important?
Interested in best practices for recruiting and retaining patient participants in research?
Do you have trouble coming up with a short, clear description of your project or idea?
Need a survey for your research project?
Looking for novel data analysis methods and tools for addiction research?
Why is it important to include older adults in research, and how can it improve your study?
How do you know which study design to choose for your project?
What is linear and logistic regression, and when should you use it?
How does stakeholder engagement work in basic science research?
Does your clinical trial qualify for insurance coverage?
Wondering how patient survival data is analyzed in clinical research?
How do you develop a research protocol that ensures the safety and confidentiality of your study participants?
Interested in learning how to incorporate Item Response Theory (IRT) in your research surveys?
What makes a journal article successful?
What is stakeholder and community engagement (SCE), and why is it important?
Need help interpreting reviews and deciding when is best to revise and resubmit?
Do you have a grant proposal or protocol for an intervention involving hospitals, schools, or local communities?
What does a researcher need to know before signing an agreement?
How can we use group data to treat individual patients?
