Ellen Mommers

Ellen Mommers Email and Phone Number

sr Clinical Project Manager @ CR2O | Clinical CRO
Netherlands
Ellen Mommers's Location
Netherlands, Netherlands
Ellen Mommers's Contact Details

Ellen Mommers work email

Ellen Mommers personal email

About Ellen Mommers

Seeking a new opportunity in a dynamic environment where I can contribute to the development of new drugs. While my expertise lies in oncology, I am open to any therapeutic area where I can make a meaningful impact on patient care.With over 20 years of clinical leadership experience in global phase I/II/III clinical trials, I am skilled in all scientific and operational aspects of clinical trials, from drafting initial protocol synopses to result reporting. I love to engage with investigators, fostering strong relationships, manage CROs and third party vendors, and lead the clinical trial team to a successful completion. But I also like to do the hands-on work and solve unforeseen issues that arise during trial set-up and execution. You will get to know me as a dedicated, open, and honest professional known for my strong oversight, analytical skills, and willingness to help others. I am eager to bring my experience to the next step in my career.

Ellen Mommers's Current Company Details
CR2O | Clinical CRO

Cr2O | Clinical Cro

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sr Clinical Project Manager
Netherlands
Website:
cr2o.nl
Employees:
18
Ellen Mommers Work Experience Details
  • Cr2O | Clinical Cro
    Sr Clinical Project Manager
    Cr2O | Clinical Cro
    Netherlands
  • Radboudumc
    Strategic Manager Pedmed-Nl
    Radboudumc Mar 2024 - Jul 2024
    Nijmegen, Nl
    Pedmed-NL is a dynamic network uniting Dutch academic and top regional hospitals to drive high-quality pediatric clinical trials. Pedmed-NL is one of the national teams of the European conect4children (c4c) initiative.As a Strategic Manager, my primary responsibilities include strengthening our network, enhancing collaboration with hospitals and other networks, and boosting the visibility of Pedmed-NL among industry stakeholders and researchers.
  • Byondis
    Director Clinical Development At Byondis
    Byondis May 2020 - Jul 2023
    As continuation of my previous role at the same company (Synthon/Byondis), leading first-in-human and phase II clinical trials in solid tumors, breast cancer, and non-Hodgkin lymphoma. Managing all scientific and operational aspects from drafting initial synopsis to final result reporting. Including selecting and engaging investigators, regulatory interactions, and CRO and vendor management.Additionally, I contributed to BLA and MAA preparation for an Antibody-Drug Conjugate (ADC), including writing modules, patient leaflets, and regulatory responses.
  • Synthon
    Senior Clinical Project Leader
    Synthon Mar 2012 - May 2020
    Nijmegen, Nl
    Senior clinical project leader in phase I oncology trials with antibody-drug conjugates. Responsible for all scientific and operational tasks in performing clinical trials. The biotech part of the company was separated in 2020 and renamed Byondis.
  • Organon/Shering-Plough/Msd
    Senior Clinical Project Scientist
    Organon/Shering-Plough/Msd May 2005 - Mar 2012
    Project and trial management in late stage clinical development. This includes writing clinical development plans, lead clinical trial teams, write clinical trial protocols (phase II, IIIa and IIIb), organize expert meetings to discuss trial design, operational management of clinical trials, write clinical trial reports, participate in scientific advice meetings with health authorities, write modules of Common Technical Document, involved in answering questions from health authorities, and write publications.Therapeutic areas: contraception, male contraception, benign prostatic hyperplasia, fertility, cachexia, sarcopenia
  • Organon
    Regulatory Affairs Scientist
    Organon Jan 2001 - May 2005
    Jersey City, Nj, Us
    Representative of regulatory affairs in Global Project Teams and Clinical Trial Teams. My responsibilities included writing Investigator Brochures, preparing target product profile, writing submission documents for Health Authorities, and involved in maintenance of marketing approvals. Therapeutic areas: antithrombotics, anesthesia, cancer.
  • Vu Amsterdam
    Phd Researcher
    Vu Amsterdam Sep 1995 - Mar 2001
    Amsterdam, Nl
    PhD in 'Preinvasive ductal breast lesions: cell biological, quantitative, and clinical aspects'(Co)Promoters: Dr. P. van Diest, Prof J. Baak, Prof C. Meijer

Ellen Mommers Skills

Clinical Development Clinical Trials Clinical Research Regulatory Affairs Gcp Drug Development Pharmaceutical Industry Clinical Study Design Ctms Life Sciences Ich Gcp Project Management Cro Program Management Women's Health Product Development Teamwork Research Project Management Clinical Clinical Trial Management Clinical Supervision Team Leadership

Ellen Mommers Education Details

  • Radboud University
    Radboud University
    Biomedical Sciences

Frequently Asked Questions about Ellen Mommers

What company does Ellen Mommers work for?

Ellen Mommers works for Cr2o | Clinical Cro

What is Ellen Mommers's role at the current company?

Ellen Mommers's current role is sr Clinical Project Manager.

What is Ellen Mommers's email address?

Ellen Mommers's email address is el****@****ail.com

What schools did Ellen Mommers attend?

Ellen Mommers attended Radboud University.

What skills is Ellen Mommers known for?

Ellen Mommers has skills like Clinical Development, Clinical Trials, Clinical Research, Regulatory Affairs, Gcp, Drug Development, Pharmaceutical Industry, Clinical Study Design, Ctms, Life Sciences, Ich Gcp, Project Management.

Who are Ellen Mommers's colleagues?

Ellen Mommers's colleagues are Bart Hendriks, Bas Ossenkoppele, Laura Van Der Leden, Cari Jacobs-Blom.

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