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Lisa Morch Location
Erin, ON, CA
Lisa Morch Work
2020 -now Clinical Study Manager @
2017 -now Study Lead Monitor @
2014 -2017 Country Lead Monitor @
2010 -2014 Senior Research Associate @
2008 -2010 Sr.Clinical Data Manager @ i3statprobe
2007 -2008 Clinical Data Editor @
2006 -2008 Clinical Data Project Manager @ Endpoint Research
2004 -2006 Data Co-ordinator @ AAIPharma
2002 -2004 Data Manager @ AAI development Services
Lisa Morch Skills
EDC
CRO
GCP
Clinical Data Management
Clinical Development
Clinical Monitoring
CTMS
Clinical Trials
Oncology
Pharmaceutical Industry
Clinical Research
Sop
Therapeutic Areas
Drug Development
ICH-GCP
Biotechnology
Electronic Data Capture (EDC)
CRO Management
Clinical Trial Management System (CTMS)
Standard Operating Procedure (SOP)
Good Clinical Practice (GCP)
Leadership
PowerPoint
Ich Gcp
Business Analysis
Strategic Planning
Microsoft Excel
Journalism
Hospitals
Clinical Trial Management System Ctms
Good Clinical Practice Gcp
Standard Operating Procedure Sop
Electronic Data Capture Edc
Good Clinical Practice
Electronic Data Capture
Clinical Trial Management System
Standard Operating Procedure
Lisa Morch Summary
Lisa Morch, based in Erin, ON, CA, is currently a Clinical Study Manager at Bayer. Lisa Morch brings experience from previous roles at Bayer, Boehringer Ingelheim and i3statprobe. With a robust skill set that includes EDC, CRO, GCP, Clinical Data Management, Clinical Development and more. Lisa Morch has 3 emails on RocketReach.
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