2019 -2021 ePRO Technical Project Manager, IRT and COA Services, Global Clinical Data Integration @ Merck via PRA Health Sciences
2017 -2019 Senior Operations Manager @
2015 -2017 Clinical Manager and Operations Manager @
2013 -2015 Clinical Operations Associate @
2012 -2013 Results and Registration Specialist @ Clinforce on Assignment for Merck
2011 -2012 Investigator Document Associate and Clinical Trial Associate @ Research Pharmaceutical Services on assignment for Johnson & Johnson
2010 -2011 Clinical Trial Associate @ ExecuPharm Inc on assignment for Pfizer
Kelly Doyle Education
Marymount University 2022-2026
Drexel University College of Medicine 2017
Chestnut Hill College 2008
Kelly Doyle Skills
Clinical Trials
CTMS
GCP
Clinical Research
Pharmaceutical Industry
Vaccines
Diabetes
CRO
Cardiology
Therapeutic Areas
Clinical Development
Oncology
Respiratory and Immunology
Project Management
ClinicalTrials.gov
SharePoint
TMF
Sop
Protocol
Clinical Operations
Trial Management
Regulatory Documentation
Clinical Study Design
Phase I
Pharmacovigilance
ICH-GCP
EDC
Regulatory Submissions
Clinical Data Management
Clinical Monitoring
Biotechnology
Customer Service
Management
Microsoft Office
Good Clinical Practice (GCP)
Clinical Trial Management System (CTMS)
Standard Operating Procedure (SOP)
CRO Management
Clinical Trial Management System Ctms
Ich Gcp
Good Clinical Practice Gcp
Standard Operating Procedure Sop
Standard Operating Procedure
Clinical Trial Management System
Good Clinical Practice
Kelly Doyle Summary
Kelly Doyle, based in Philadelphia, PA, US, is currently a Director, Licensing and Translations: Clinical Outcomes Assessments and Copyrights at Merck. Kelly Doyle brings experience from previous roles at Merck and Merck via PRA Health Sciences. Kelly Doyle holds a 2022 - 2026 Marymount University. With a robust skill set that includes Clinical Trials, CTMS, GCP, Clinical Research, Pharmaceutical Industry and more. Kelly Doyle has 1 emails and 1 mobile phone numbers on RocketReach.
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