Suzanne Hendriksen Email and Phone Number
Suzanne Hendriksen work email
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Suzanne Hendriksen personal email
I'm a passionate pharma professional with 25 years experience in Regulatory Affairs in innovative drug development up to market approval worldwide. I gained my expertise is in Regulatory leadership and strategy roles focussing on Health Authority engagement in an international biotech/pharma environment. With broad knowledge of the various fields within drug development, i.e. CMC/quality, nonclinical and clinical.I am an engaged teamplayer and -leader who likes to build, facilitate and motivate a team throughout all types of circumstances within the product's lifecycle. My motto: Thinking in solutions and together make it happen!I can provide strategic advice and support for the best development and regulatory pathway and tailor this to the respective type of product and disease area, taking into account the business and patient needs. This also includes risk management, process improvements and optimising interdepencies for timely and high quality deliverables.As a strategic teamplayer I connect and engage people in cross-functional project teams to create regulatory submissions for product through all phases of pharmaceutical development, and communicate these with EMA (FDA) and national Health Authorities as well as take care of the internal stakeholder communication. My project management background in multidisciplinary matrix organisations in pharma industry, allows me to manage planning and content of dossier deliverables, connecting and inspiring all stakeholders to achieve the same goal. Team commitment and a clear common goal are in my view essential in this process.
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Sr. Dir. Regulatory Affairs EuropeBristol Myers Squibb Nov 2020 - PresentUtrecht, Nederland -
Head Regulatory Affairs EuMyokardia Apr 2020 - Oct 2020Amsterdam, Noord-Holland, Nederland -
Associate Director Regulatory AffairsGenzyme Europe B.V. Jun 2015 - Apr 2020Naarden, The Netherlands -
Director Quality And Regulatory AffairsMytomorrows.Com Feb 2014 - May 2015Amsterdam Area, Netherlands -
Head Of Regulatory Affairs BiopharmaceuticalsSynthon Nov 2011 - Jan 2014Nijmegen Area, Netherlands -
Senior Director Regulatory AffairsPharming Jan 2008 - Nov 2011 -
Senior ConsultantXendo Pharma Services Mar 2005 - Dec 2007 -
Regulatory Affairs ManagerN.V. Organon Apr 2003 - Feb 2005responsible for regulatory authority contact with respect to products marketing approvalsinternal communication/coordination of required (regulatory/scientific) information -
Regulatory Affairs ScientistN.V. Organon Mar 1999 - Apr 2003give strategic regulatory input in international multidisciplinary project teams.Development of NCEs and biotech productsCMC, nonclinical and clinical input in different positionsinternational regulatory project teamleader
Suzanne Hendriksen Skills
Suzanne Hendriksen Education Details
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Bio-Pharmaceutical Sciences
Frequently Asked Questions about Suzanne Hendriksen
What company does Suzanne Hendriksen work for?
Suzanne Hendriksen works for Bristol Myers Squibb
What is Suzanne Hendriksen's role at the current company?
Suzanne Hendriksen's current role is Sr. Dir. Regulatory Affairs Europe.
What is Suzanne Hendriksen's email address?
Suzanne Hendriksen's email address is su****@****yme.com
What schools did Suzanne Hendriksen attend?
Suzanne Hendriksen attended Universiteit Leiden.
What skills is Suzanne Hendriksen known for?
Suzanne Hendriksen has skills like Regulatory Affairs, Regulatory Submissions, Pharmaceutical Industry, Biotechnology, Biopharmaceuticals, Clinical Trials, Clinical Development, Lifesciences, Fda, Drug Development, Pharmaceutical Development, Strategy.
Who are Suzanne Hendriksen's colleagues?
Suzanne Hendriksen's colleagues are Francesco Rao, Rahul Kuraichya, Gina M., Morwehrene Yalartai, Joe V., Robert Lokken Jr., Denny Lai.
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