Suzanne Hendriksen Email & Phone Number

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.

Listed skills include Regulatory Affairs, Regulatory Submissions, Pharmaceutical Industry, Biotechnology, and 13 others.

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  Universiteit Leiden

  Bio-Pharmaceutical Sciences