2011 -2012 Pharmacovigilance and Regulatory Consultant @
2010 -2011 Senior Drug Safety Analyst US Product Surveillance @
2009 -2010 Clinical Safety Specialist and Medical Project Manager @
2007 -2009 Drug Safety Associate @
2005 -2007 Clincial Research Coordinator @
1995 -2005 Paramedic @
2000 -2005 HM2 - Corpsman @
1991 -1995 Paramedic @ New York City EMS
1988 -1991 Paramedic @
Maureen Quirk Education
Northeastern University
MS (Regulatory Affairs for Drugs, Devices, and Biologics)
2008-2010
Maureen Quirk Skills
Team Leadership
Data Entry
Project Management
Goal Setting
Cross-team Collaboration
Operations Management
Training
Leadership
Pharmaceutical Research
Oncology Clinical Research
Patient Safety
Healthcare
Clinical Trials
GCP
Regulatory Affairs
Pharmaceutical Industry
Pharmacovigilance
Clinical Research
Oncology
Clinical Development
CTMS
FDA
Drug Safety
CRO
Biotechnology
Sop
Medical Devices
Cardiology
21 CFR Part 11
Biopharmaceuticals
Clinical Data Management
Clinical Operations
Drug Development
GLP
GxP
ICH-GCP
IND
Infectious Diseases
MedDRA
Medical Affairs
Medical Writing
Medicine
Neurology
Pharmaceutics
Regulatory Submissions
Therapeutic Areas
Veterans
CRO Management
Good Clinical Practice (GCP)
Ich Gcp
EMS
Good Clinical Practice Gcp
Operations
Good Clinical Practice
Maureen Quirk Summary
Maureen Quirk, based in Bridgeville, DE, US, is currently a Pharmacovigilance Consultant at Confidential ( Stealth Mode ). Maureen Quirk brings experience from previous roles at AVEO Oncology, HealthCore, Inc. and Apellis Pharmaceuticals. Maureen Quirk holds a 2008 - 2010 MS in Regulatory Affairs for Drugs, Devices, and Biologics @ Northeastern University. With a robust skill set that includes Team Leadership, Data Entry, Project Management, Goal Setting, Cross-team Collaboration and more. Maureen Quirk has 1 emails and 1 mobile phone numbers on RocketReach.
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