Maureen Quirk Email & Phone Number
Pharmacovigilance Consultant @ Confidential ( Stealth Mode )
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Maureen Quirk Location
- Bridgeville, DE, US
Maureen Quirk Work
- Pharmacovigilance Consultant @ (April 2023 - Present)
- Director Pharmacovigilance Operations @ (April 2022 - April 2023)
- Director Pharmacovigilance Operations @ (March 2021 - March 2022)
- Director, Global Pharmacovigilance Operations @ (September 2020 - March 2021)
- Senior Manager, Pharmacovigilance Operations @ (November 2019 - September 2020)
- Senior Pharmacovigilance Consultant @ (January 2017 - August 2019)
- Senior Manager, Pharmacovigilance Operations @ (July 2016 - November 2016)
- Clinical PV Operations Manager @ (April 2016 - July 2016)
- Senior Pharmacovigilance Submission Specialist @ (July 2015 - April 2016)
- Senior Pharmacovigilance Specialist @ (September 2014 - July 2015)
- Safety Surveillance Monitor @ Telerx (formerly Sentrx) (December 2012 - September 2014)
- Senior Drug Safety Specialist @ (July 2012 - October 2012)
- Pharmacovigilance and Regulatory Consultant @ (November 2011 - June 2012)
- Senior Drug Safety Analyst US Product Surveillance @ (August 2010 - November 2011)
- Clinical Safety Specialist and Medical Project Manager @ (October 2009 - August 2010)
- Drug Safety Associate @ (March 2007 - October 2009)
- Clincial Research Coordinator @ (October 2005 - March 2007)
- Paramedic @ (January 1995 - October 2005)
- HM2 - Corpsman @ (January 2000 - December 2005)
- Paramedic @ New York City EMS (January 1991 - December 1995)
- Paramedic @ (January 1988 - December 1991)
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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