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Irena Lambridis
Irena Lambridis
VP, Head of Global Quality Assurance & Compliance and Regulatory Affairs | Science 37
Florida, United States
Irena Lambridis
Summary
Irena Lambridis is a seasoned professional in the biopharmaceutical and clinical research sectors, currently serving as the VP, Head of Global Quality Assurance & Compliance and Regulatory Affairs at Science 37. With extensive experience in managing multi-center Phase I-IV clinical trials across various therapeutic areas including oncology and cardiology, Irena has a proven track record in ensuring regulatory compliance and quality assurance. Her expertise encompasses a wide range of clinical operations, from protocol development to regulatory submissions, underpinned by her strong foundation in regulatory affairs and quality assurance practices. Irena has held leadership roles in several organizations, demonstrating her ability to lead diverse teams and drive process improvements. Her commitment to excellence in clinical research is evident in her strategic approach to quality management and compliance. Beyond her professional pursuits, Irena is passionate about advancing clinical research practices through innovation and collaboration.
Irena Lambridis
Work Experience
VP, Head of Global Quality Assurance & Compliance and Regulatory Affairs at
Science 37
April 2023 - Present
Head of Global Quality Assurance, Compliance and Corporate Training at
KCR
June 2022 - April 2023
Director Clinical Quality Assurance & Compliance (and KCR Learning & Development) at
KCR
January 2019 - June 2022
Program Manager, Clinical Global Quality (Auditing) & Compliance at
Iqvia Biotech
October 2017 - January 2019
Senior Clinical Quality Assurance GCP Auditor at
Chiltern
July 2016 - October 2017
Clinical Quality & Compliance / Quality Assurance Auditor at
Novella Clinical
January 2007 - July 2016
Manager, Investigator Strategy & Site Coordination at
Novella Clinical
January 2007 - January 2013
Document Control Specialist, Regulatory Affairs at
Novella Clinical
January 2007 - January 2012
Department Lead: Investigator Strategy & Site Coordination at
Novella Clinical
January 2007 - January 2012
Regulatory Affairs Specialist and Process Improvement (Lean Six Sigma) Coordinator at
Novella Clinical
January 2007 - January 2011
Clinical Trial Associate; Regulatory Inspection Team at
i3 Research
January 2010 - January 2011
Study Start-Up Associate at
Novella Clinical
January 2007 - January 2008
Irena Lambridis
Education
RAPS Regulatory Affairs, Regulatory Affairs Certificiation
January 2012 - January 2013
Frequently Asked Questions about Irena Lambridis
What is Irena Lambridis email address?
Irena Lambridis's primary email address is ***************@science37.com. To view the full verified email and additional contact details, sign up for free with Muraena.
What company does Irena Lambridis work for?
Irena Lambridis is a VP, Head of Global Quality Assurance & Compliance and Regulatory Affairs at Science 37, a company specializing in Commercial physical research.
Where Irena Lambridis graduated from?
Irena Lambridis holds a degree in from RAPS Regulatory Affairs.
How can I directly contact Irena Lambridis?
To contact Irena Lambridis directly, you can use the email address ***************@science37.com. Complete contact information is available upon registration with Muraena.
Who is Irena Lambridis?
Irena Lambridis is a seasoned professional in the biopharmaceutical and clinical research sectors, currently serving as the VP, Head of Global Quality Assurance & Compliance and Regulatory Affairs at Science 37. With extensive experience in managing multi-center Phase I-IV clinical trials across various therapeutic areas including oncology and cardiology, Irena has a proven track record in ensuring regulatory compliance and quality assurance. Her expertise encompasses a wide range of clinical operations, from protocol development to regulatory submissions, underpinned by her strong foundation in regulatory affairs and quality assurance practices. Irena has held leadership roles in several organizations, demonstrating her ability to lead diverse teams and drive process improvements. Her commitment to excellence in clinical research is evident in her strategic approach to quality management and compliance. Beyond her professional pursuits, Irena is passionate about advancing clinical research practices through innovation and collaboration.
Irena`s contact details
***************@science37.com
***************@kcrcro.com
**********@novellaclinical.com
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