Maurice Green Rasmussen
A multilingual professional Director, with 17 years of demonstrated history of leadership in the Global Regulatory and Clinical... | New York, New York, United States
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Maurice Green Rasmussen’s Emails mg****@no****.com
Maurice Green Rasmussen’s Phone Numbers No phone number available.
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Maurice Green Rasmussen’s Location New York, New York, United States
Maurice Green Rasmussen’s Expertise A multilingual professional Director, with 17 years of demonstrated history of leadership in the Global Regulatory and Clinical Operations fields. Strong experience in the biotechnology and pharmaceutical industry. In my current role, I lead the regulatory and clinical strategies along with the TMF and asset transfer teams, for 3 major Oncology filings (MAA, CTA) to the EMA and MHRA. Overseeing the planning, execution, and delivery of multiple clinical trials and programs across different therapeutic areas and stages of development. I also collaborate with internal and external stakeholders, such as regulatory agencies, CROs, vendors, and investigators, to ensure compliance, quality, and efficiency of the clinical operations and data management. Some of my key achievements include successfully managing the document management transition of several assets from partner companies to EQRx Inc. and from EQRx Inc. to partners. Implementing best practices and standards for clinical operations and data management, and contributing to the submission of regulatory filings. Skilled in Good Clinical Practice (GCP), regulatory requirements, master data management, and project management, as well as global Health Authorities (HA) filings and interactions (FDA, EMA, PMDA, etc.).
Maurice Green Rasmussen’s Current Industry Eqrx
Maurice
Green Rasmussen’s Prior Industry
Novo Nordisk
|
Ovid Therapeutics
|
Aavantibio
|
Eqrx
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Work Experience
Eqrx
Director, Clinical Operations and Asset Transfer Managem
Thu Jun 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Eqrx
Associate Director, Clinical Operations -Asset Transfer
Sat Jan 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jun 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time)
Aavantibio
Associate Director, Regulatory Affairs Program Manage
Mon Mar 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Jan 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time)
Ovid Therapeutics
Global Regulatory Affairs Associate Director
Thu Aug 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Apr 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)
Novo Nordisk
Regulatory Affairs Specialist
Sun May 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Jul 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time)
Novo Nordisk
Associate Manager
Wed Jan 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun May 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time)
Novo Nordisk
Senior Regulatory Associate
Tue Mar 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Dec 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time)
Novo Nordisk
Regulatory Affairs Associate
Thu Jan 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Jan 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time)
Novo Nordisk
VP Assistant
Mon Jan 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jan 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time)Skills
Languages
Maurice Green Rasmussen Email Addresses
FAQ About Maurice Green Rasmussen
-
Maurice Green Rasmussen is located at
New York, New York, United States -
Maurice Green Rasmussen is a
A multilingual professional Director, with 17 years of demonstrated history of leadership in the Global Regulatory and Clinical Operations fields. Strong experience in the biotechnology and pharmaceutical industry. In my current role, I lead the regulatory and clinical strategies along with the TMF and asset transfer teams, for 3 major Oncology filings (MAA, CTA) to the EMA and MHRA. Overseeing the planning, execution, and delivery of multiple clinical trials and programs across different therapeutic areas and stages of development. I also collaborate with internal and external stakeholders, such as regulatory agencies, CROs, vendors, and investigators, to ensure compliance, quality, and efficiency of the clinical operations and data management. Some of my key achievements include successfully managing the document management transition of several assets from partner companies to EQRx Inc. and from EQRx Inc. to partners. Implementing best practices and standards for clinical operations and data management, and contributing to the submission of regulatory filings. Skilled in Good Clinical Practice (GCP), regulatory requirements, master data management, and project management, as well as global Health Authorities (HA) filings and interactions (FDA, EMA, PMDA, etc.). Eqrx -
Maurice Green Rasmussen currently works in the
Eqrx -
Maurice Green Rasmussen specializes in
A multilingual professional Director, with 17 years of demonstrated history of leadership in the Global Regulatory and Clinical Operations fields. Strong experience in the biotechnology and pharmaceutical industry. In my current role, I lead the regulatory and clinical strategies along with the TMF and asset transfer teams, for 3 major Oncology filings (MAA, CTA) to the EMA and MHRA. Overseeing the planning, execution, and delivery of multiple clinical trials and programs across different therapeutic areas and stages of development. I also collaborate with internal and external stakeholders, such as regulatory agencies, CROs, vendors, and investigators, to ensure compliance, quality, and efficiency of the clinical operations and data management. Some of my key achievements include successfully managing the document management transition of several assets from partner companies to EQRx Inc. and from EQRx Inc. to partners. Implementing best practices and standards for clinical operations and data management, and contributing to the submission of regulatory filings. Skilled in Good Clinical Practice (GCP), regulatory requirements, master data management, and project management, as well as global Health Authorities (HA) filings and interactions (FDA, EMA, PMDA, etc.). -
Maurice Green Rasmussen speaks the following languages:
No languages available. -
Maurice Green Rasmussen has prior experience in the following industries:
Eqrx , Aavantibio , Ovid Therapeutics , Novo Nordisk , Novo Nordisk , Novo Nordisk , Novo Nordisk , Novo Nordisk -
Maurice Green Rasmussen has the following professional experience:
Eqrx , Eqrx , Aavantibio , Ovid Therapeutics , Novo Nordisk , Novo Nordisk , Novo Nordisk , Novo Nordisk , Novo Nordisk . -
You can view Maurice Green Rasmussen’s
LinkedIn profile at LinkedIn URL. -
Maurice Green Rasmussen’s work email addresses are
[email protected] . -
Maurice Green Rasmussen works at
Eqrx
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