Kirsten Morasco leads GXP compliance activities for CIS. Kirsten and her team have assisted clients with process development, compliance documentation development, GCP and Compliance Training development and delivery, GXP audit, and Vendor Oversight Program development.
Kirsten brings over 19 years of experience in the pharmaceutical industry to her role at CIS. Kirsten began her career in clinical operations as a clinical trial manager and monitor. Following her role in clinical operations she moved into the field of consulting where she has assisted clients with process improvement, process documentation, training and GCP compliance. She joined CIS in 2012 and specializes in global process consulting, change management and team building.
Kirsten graduated with a Bachelor of Science degree in Biology from The Catholic University of America.