Research Integrity and Clinical Operations

Our commitment to best practices across the wide range of clinical research and trials at UMass relies on attention to ethics, regulatory knowledge and clinical and participant resources.  The integration of these three areas ensures that compliance with human research protection is always paramount, with reliable and accessible resources and services available to investigators and their staff for safe and efficient study activities across the life cycle of their research. 

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For more details or further information about Research Integrity and Clinical Operations, please call Sheila Noone, PhD at 508-856-5015 or email sheila.noone@umassmed.edu

Clinical Research Ethics

Regulatory Knowledge and Support

Clinical and Participant Resources

 

 

Sign-up for UMCCTS Membership

 Benefits

  • Pilot grant programs eligibility
  • Research core services
    at competitive rates
  • Electronic resources access at Amherst libraries
  • Medical School Library access
  • Consultation services
  • Notification of special events and opportunities

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