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Irena Lambridis

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Irena Lambridis

VP, Head of Global Quality Assurance & Compliance and Regulatory Affairs | Science 37

Florida, United States

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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.

General

Specialist

Technical Background

Leadership Experience

Long-Term Tenure

Professional interests

Leadership Development

Innovation

Organisational experience

Corporate Experience

Consulting Experience

Irena Lambridis

Work Experience

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VP, Head of Global Quality Assurance & Compliance and Regulatory Affairs at

Science 37

April 2023 - Present

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Head of Global Quality Assurance, Compliance and Corporate Training at

KCR

June 2022 - April 2023

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Director Clinical Quality Assurance & Compliance (and KCR Learning & Development) at

KCR

January 2019 - June 2022

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Program Manager, Clinical Global Quality (Auditing) & Compliance at

Iqvia Biotech

October 2017 - January 2019

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Senior Clinical Quality Assurance GCP Auditor at

Chiltern

July 2016 - October 2017

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Clinical Quality & Compliance / Quality Assurance Auditor at

Novella Clinical

January 2007 - July 2016

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Manager, Investigator Strategy & Site Coordination at

Novella Clinical

January 2007 - January 2013

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Document Control Specialist, Regulatory Affairs at

Novella Clinical

January 2007 - January 2012

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Department Lead: Investigator Strategy & Site Coordination at

Novella Clinical

January 2007 - January 2012

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Regulatory Affairs Specialist and Process Improvement (Lean Six Sigma) Coordinator at

Novella Clinical

January 2007 - January 2011

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Clinical Trial Associate; Regulatory Inspection Team at

i3 Research

January 2010 - January 2011

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Study Start-Up Associate at

Novella Clinical

January 2007 - January 2008

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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

mail

***************@science37.com

***************@kcrcro.com

**********@novellaclinical.com

Colleagues

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Mike Zaranek

Chief Financial Officer

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David Coman

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Jonathan Cotliar

Chief Medical Officer

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Casey Beckwith

Vice President, FP&A

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Westley King

Chief Financial Officer

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Tyler Van Horn

Chief Commercial Officer (CCO)

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