Erik Van Leeuwen, M.Sc, Pmp Email and Phone Number
Erik Van Leeuwen, M.Sc, Pmp work email
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Erik Van Leeuwen, M.Sc, Pmp personal email
I have over 20 years’ Clinical Development experience in a broad range of activities. Vast experience in clinical trials (Ph I, Ph II, Ph III, Phase IV, including IIS and RWE), Project, Portfolio and Line-Management, several process improvement initiatives and management of clinical operations teams. Under my leadership, Abbott gained NDA approval in China for one of our key products in 2020, while NDA's for two other products were submitted by end 2019 in China as well.I have expertise working with and leading global and virtual teams. In the past years I have specialized managing clinical trials in Asia and gained experience working with Asian team members. I have successfully delivered projects in the environment of Asian/Chinese working culture. Same expertise for Eastern Europe region including Russia. As PMP certified Project Manager, I am committed to assure teams deliver projects successfully, in time and on budget. In order to achieve this, I cooperate well with my team and execute stakeholder management easily throughout several layers in Governance Structures. Next to working in a commercial environment, I am interested in contributing to society, which I have done as chair of a local community interest organization.
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Qa Manager, Head Of Qa Department At Rivm, DvpRivm National Institute For Public Health And The EnvironmentDen Dolder, Ut, Nl -
Manager, Global Clinical OperationsAbbott Sep 2020 - PresentWeesp, North Holland, NetherlandsManager Clinical Programs leads the clinical operational aspects of clinical development programs.Providing overall clinical operational direction and ensuring functional alignment of the clinical study teams within overall strategy, goals and objectives of the respective clinical programs.Six Direct Reports; (senior) Clinical Trial Managers. -
Senior Clinical Project ManagerAbbott Laboratories Sep 2012 - Aug 2020Weesp, The NetherlandsCoordination of compound development & registration, from start of Phase I clinical trials up to NDA submission. Investigator Sponsored Studies.Leading multidisciplinary teams.CRO management/oversight.Excellent communicator throughout governance structure.Leading several process improvement projects.Significant contributor to the successful submission of the registration dossier for IVF indication for Dydrogestrone in EMA and Russia (see link below).Team Lead of Chinese Authorities (NMPA) inspections, resulting in NDA approval Dydrogestrone for IVF indication China. -
Senior Clinical Trial ManagerSolvay Pharmaceuticals Sep 2002 - Sep 2012Amsterdam Area, NetherlandsManaging the process of clinical trials conduct within Alliance CRO-Sponsor setting ensuring effective co-ordination of all clinical activities in phase II, III and IV trials.Supervise local study Abbott CTM’s in a large Parkinson Disease program.
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Alliance Communication ManagerSolvay Pharmaceuticals Jan 2009 - Dec 2010Team lead of the Quintiles – Solvay Alliance Communication Group (five people). Mission of this group is to help Alliance Management and the general alliance community to achieve the successful execution of alliance strategy via timely sharing of the relevant alliance information.
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CraiiCentocor Feb 1999 - Aug 2002*CRAII for large phase III cardiovascular trials (set up, initiation and execution):*Initiate and maintain Centocor database with regulatory submission information European countries.*Involved in general Centocor activities. E.g. writing SOP’s, buddy new employees, initiating and maintaining ergonomy project, assisting in design time-management system. -
CraBoehringer Ingelheim Pharmaceuticals Mar 1997 - Feb 1999 -
In House CraCardialysis 1996 - 1997
Erik Van Leeuwen, M.Sc, Pmp Education Details
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Medical Biology -
Sint MaartenscollegeVwo
Frequently Asked Questions about Erik Van Leeuwen, M.Sc, Pmp
What company does Erik Van Leeuwen, M.Sc, Pmp work for?
Erik Van Leeuwen, M.Sc, Pmp works for Rivm National Institute For Public Health And The Environment
What is Erik Van Leeuwen, M.Sc, Pmp's role at the current company?
Erik Van Leeuwen, M.Sc, Pmp's current role is QA Manager, Head of QA department at RIVM, DVP.
What is Erik Van Leeuwen, M.Sc, Pmp's email address?
Erik Van Leeuwen, M.Sc, Pmp's email address is er****@****ott.com
What schools did Erik Van Leeuwen, M.Sc, Pmp attend?
Erik Van Leeuwen, M.Sc, Pmp attended Utrecht University, Sint Maartenscollege.
Who are Erik Van Leeuwen, M.Sc, Pmp's colleagues?
Erik Van Leeuwen, M.Sc, Pmp's colleagues are Charlotte Goldhoorn, Peter Bos, Marjolein Weda, Manon Savelkoul, Michelle Stadlander, Anne Buitenhuis, Ariejaak Verkade.
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