Kelly Doyle Email & Phone Number
Director, Licensing and Translations: Clinical Outcomes Assessments and Clinical Copyrights @ Merck
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Kelly Doyle Location
- Philadelphia, PA, US
Kelly Doyle Work
- Director, Licensing and Translations: Clinical Outcomes Assessments and Clinical Copyrights @ (February 2025 - Present)
- Director, Clinical Outcomes Assessments, Licensing, and Translations @ (November 2024 - Present)
- Associate Director, Clinical Outcomes Assessments, Licensing and Translations @ (December 2022 - November 2024)
- Senior, Clinical Outcomes Assessments, COA Services, eClinical Technologies @ (August 2021 - December 2022)
- ePRO Technical Project Manager, IRT and COA Services, Global Clinical Data Integration @ Merck via PRA Health Sciences (April 2019 - August 2021)
- Senior Operations Manager @ (October 2017 - April 2019)
- Clinical Manager and Operations Manager @ (June 2015 - October 2017)
- Clinical Operations Associate @ (June 2013 - June 2015)
- Results and Registration Specialist @ Clinforce on Assignment for Merck (February 2012 - June 2013)
- Investigator Document Associate and Clinical Trial Associate @ Research Pharmaceutical Services on assignment for Johnson & Johnson (May 2011 - January 2012)
- Clinical Trial Associate @ ExecuPharm Inc on assignment for Pfizer (July 2010 - May 2011)
Kelly Doyle Education
- Marymount University
Doctorate in Business Administration in Business Intelligence and Technology
2022-2026 - Drexel University College of Medicine
Masters of Science (Clinical Research Organization and Management)
2017 - Chestnut Hill College
BS in Business Admin (Business Administration)
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 Clinical Copyrights at Merck. Kelly Doyle brings experience from previous roles at Merck and Merck via PRA Health Sciences. Kelly Doyle holds a 2022 - 2026 Doctorate in Business Administration in Business Intelligence and Technology @ 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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