PSG Research Coordinator Resource Listing

We realize how hard the job of a coordinator is, and we would like to help make your lives just a little bit easier. We have pooled a premier group of PSG coordinators together to help answer any and all of your questions. You can review the list below along with their featured areas of expertise and contact information.

Karen Williams, BA, CCRP
Northwestern University, Dept. of Neurology
710 N. Lake Shore Drive, 11th Fl
Chicago, IL 60611
(312) 503-5645 (office)
(312) 503-0787 (fax)
k-willliams8@northwestern.edu
• Training/on-boarding new research staff
• Monitoring preparation
• Retention/Recruitment
• Collaborating with Ancillary Depts

Cindy Casaceli, MBA
DirectorClinical Trials Coordination Center
Center forHealth + Technology (CHeT)
University of Rochester
(585) 273-4239
• Clinical Trial Operations
• Trial budgets/Per subject fee
• Data Management
• Data sharing/Data mining
• eConsent
• Telehealth
• Mobile technologies

Sarah Wong, PhD, CCRP
Clinical Research Manager, Neurology
UCSF Movement Disorders and Neuromodulation Center
San Francisco VA Medical Center
(415) 353-7885
(415) 353-9060 (Fax)
• Clinical Trials Operations
• Project Management

Melissa A. Kostrzebski
Senior Project Manager
Clinical Trials Coordination Center
Center for Health + Technology (CHeT)
University of Rochester
(585) 273-4239
melissa.kostrzebski@chet.rochester.edu
• Clinical Trial Operations
• Project Management Monitoring
• Telehealth
• Sensor Technologies
• Protocol and Consent Development
• Recruitment and Outreach
• Data entry / query management

Ray James, BS, RN
Boston University School of Medicine
Department of Neurology
Parkinson Disease and Movement Disorder Center
72 East Concord Street, C3
Boston, MA 02118
(617) 638-7745
(617) 638-5354 (Fax)
• Research Nursing activities
• PD Medications
• Motor function assessments
• Retention/Recruitment
• Preparationfor Monitor Visits
• Cross-Disciplinary Coordination
• Managing Study Budgets
• Training New Research Staff
• Visit Preparation and Source Creation
• SOP development
• Monitoring Preparation

April Langhammer, BA, CCRP
University of Kansas Medical Center
3599 Rainbow Blvd.
Kansas City, KS 66160
(913) 588-6989 (office)
alanghammer@kumc.edu
• Source document creation
• Regulatory preparation

Julia Spears, CCRC
The University of Toledo, Dept. of Neurology
Gardner-McMaster Parkinson Research Center
3000 Arlington Avenue, MS 1083
Toledo, OH 43614-2598
(419) 383-6728 (office)
(419) 383-3063 (fax)
(419) 450-9793 (cell)
julia.spears@utoledo.edu
• Budget development and negotiation
• Study start-up / essential documents
• Regulatory management
• Consent form development
• WIRB submissions
• Data entry / query management
• CRO/CRA and Sponsor relations
• Site template development (Regulatory and source)

Alistair Glidden, BA
Center for Health + Technology
University of Rochester
• Digital and decentralized/virtual trials, including participant and investigator support for telemedicine
• Subject recruitment, including social media advertising and video production
• Training and onboarding new staff
• Database design, including general considerations (question/response/report structure) and specific guidance (REDCap)atea