14 March - 15:00 -16:00 GMT / 16:00 – 17:00 CET
The evolving environment of Regulatory Affairs - an insight into the career paths of regulatory professionals at Roche
Explore the mission and role of a regulatory professional, gaining a deeper understanding of the high level interaction between the industry and external political environment. Discover the complex diversity of tasks and roles that could await you in a regulatory career.
Listen to real-life career paths and gain some insight into career development opportunities at Roche.
Audience
This Webinar will be suitable for those:
- Who are new to regulatory affairs
- Who wish to move into a role in regulatory affairs
- Who want to gain a better insight into the regulatory changing environment from an Industry perspective
Speakers
Aurelie Gaudard is Regulatory Senior Program Director and a Regulatory Ophthalmology Portfolio and Community Lead at F. Hoffmann-La Roche Ltd in Basel, Switzerland. Aurélie has over 15 years of regulatory expertise with experience worldwide, covering multiple aspects (labeling , maintenance, registration and early regulatory activities). She holds a PharmD and a PhD in Clinical Pharmacokinetics from Montpellier University, France. She started her career as a hospital pharmacist in France before joining the Pharmaceutical Industry about 20 years ago, initially in the pharmacovigilance and clinical trials fields before moving to regulatory affairs.
Elmar Wegener is EU Regulatory Intelligence Lead at F. Hoffmann-La Roche Ltd in Basel, Switzerland. Elmar has more than 15 years experience in the pharmaceutical industry. He started his career in research and development moving into regulatory affairs in 2012. Since then he has been working in different companies in global and local functions including regulatory program management, global labeling, affiliate regulatory affairs and regulatory intelligence. Currently, he is a member of the global regulatory policy and regulatory intelligence chapter leadership team at Roche. Elmar holds a MSc in Biochemistry, a PhD in molecular biology and a postgraduate MSc in Regulatory Affairs.
Paolo Marcarino is Regulatory Program Director at F. Hoffmann-La Roche Ltd in Basel, Switzerland. Paolo has over 14 years of regulatory expertise in multiple disciplines and with different regional responsibilities. In addition, he is one of the coordinators of the trainee program in Regulatory Affairs in Basel. Paolo holds a MSc degree in Medicinal Chemistry and Pharmaceutical Technology and a PhD in Pharmaceutical Sciences from Turin University (Italy).
This webinar is sponsored by
Roche.
Disclaimer: Whilst TOPRA is running this webinar for Roche, this is not an endorsement of Roche, Roche's affiliates, employees or its products and services. TOPRA is also not responsible for the content or views expressed during the webinar.
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Pricing
- Members: free
- Non-members: free
Terms and Conditions
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