All MICHR Support
Search
Filter By
Categories
Offerings available to:
Free
Connect with epidemiologists, biostatisticians, data analysts, and data scientists across U-M to enhance your health research outcomes
Free
Delineates the systematic storage, tracking and retrieval of clinical research records
Free
Consultation with behavioral research experts for tailored guidance and connection to behavioral research resources
Initial consultations are free. Staff statisticians are available at $90/hour for short-term projects or on an FTE basis for longer-term projects, such as clinical trials.
Engage with data analysis experts to ensure rigor in your clinical and translational research
Free
Conference presentations on how researchers can use AI in behavioral and digital health
Free
A presentation on considerations for capturing and analyzing racial, ethnic, and gender identity data
Range from $50 – $326 per hour (detailed breakdown under “What is this offering?”)
Supports outcome assessments for clinical trials that include measures of development, cognition, quality of life, adaptive functioning, and mental health
Free
Comprehensive assistance that ensures your clinical trials meet public and regulatory standards on time
Free
Co-creation sessions to help turn research insights into practical solutions that align with user needs
Free
A workshop that will build your capacity to work in a high-performing, cross-disciplinary team
Free
Presentations about community-engaged research methods with content adapted to audience needs
Facilitator cost, studio supplies, and staff time are covered by MICHR. Research teams are asked to pay for expert compensation.
Interactive session where researchers can enhance their projects with input from patients, caregivers, health care providers and community members
Free
Consultation to facilitate research participation by reducing potential barriers to participation and making research opportunities more accessible
Free
Participatory workshop to practice communication skills for obtaining valid informed consent