2011 -2014 Deputy QPPV and Regulatory Affairs Officer @
2010 -2011 Regulatory Administrator @
2010 -2010 Scuba Diving Instructor @
2009 -2010 Analytical Scientist @
2007 -2009 Development Analyst @
Jack O'Reilly Education
The Open University
Master of Science (MSc) (Medicinal Chemistry)
2013-2015
The Open University
BSc Hons (Life Sciences)
2008-2012
Jack O'Reilly Skills
Pharmacovigilance
Regulatory Affairs
Sop
Pharmaceutical Industry
GMP
Medical Devices
Regulatory Submissions
Regulatory Requirements
Clinical Development
FDA
CRO
Clinical Trials
Change Control
Biotechnology
eCTD
CAPA
Biopharmaceuticals
Lifesciences
Oncology
Technology Transfer
Team Leadership
Project Management
Training
Risk Management
Team Mentoring
Standard Operating Procedure (SOP)
Pharmaceutics
Good Clinical Practice (GCP)
Quality System
Management
Good Clinical Practice Gcp
Biosimilars
Launches
Drug Safety
Standard Operating Procedure Sop
See 10+See Less
Standard Operating Procedure
Good Clinical Practice
Jack O'Reilly Summary
Jack O'Reilly, based in Berlin, DE, is currently a Director of Clinical Safety and Pharmacovigilance at Medpace. Jack O'Reilly brings experience from previous roles at ProPharma Group, PV O'Reilly Ltd, Intercept Pharmaceuticals and GW Pharmaceuticals plc. Jack O'Reilly holds a 2013 - 2015 Master of Science (MSc) in Medicinal Chemistry @ The Open University. With a robust skill set that includes Pharmacovigilance, Regulatory Affairs, Sop, Pharmaceutical Industry, GMP and more. Jack O'Reilly has 2 emails and 1 mobile phone numbers on RocketReach.
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