Regulatory Science and Policy Associate - VIE Contract

Beschreibung:

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address.

At Sanofi diversity and inclusion is foundational to how we operate and is embedded in our Core Values. We respect the diversity of our people, their backgrounds and experiences. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our employees, patients and customers.

We are looking for a candidate for a VIE mission:

Regulatory Science and Policy Associate - VIE Contract

Target start date: 01/09/2024

Responsibilities:
* Analyze and synthesize emerging health authority policies and trade association activities in nominated priority areas to keep management abreast on macro trends that could impact Sanofi business.
* Drive effective and efficient collaborative efforts on regulatory science and policy matters across Sanofi teams and functions and proactively develop strategies to address future issues on priority meetings.
* Facilitate and coordinate comments on certain regulatory legislative initiatives and guidelines via SOV.
* Deliver tools and materials (e.g. position papers, talking points, scientific publications) on assigned EU policy topics that help ensure Sanofi positions and advocacy strategies for priority policy topics for the EU region are head and acted on externally.
* Represent Sanofi on a Trade Association (EFPIA/EUCOPE) working group providing positioning into industry-wide activities.
* Support RSP (Regulatory, Science and Policy) EU team in delivering Policy priorities defined for EU including ongoing activities relating to the revision of the General Pharmaceutical Legislation.
* Support coordination of GRA external engagement activities in events/conferences (DIA, TOPRA, RAPS).

Key "MUST HAVE" competencies, skills & experiences:
* Master's Degree in Pharmacy, Health Sciences, Life Sciences, Regulatory Policy, or similar.
* Previous experience in Regulatory field would be an asset.
* Self-starting and self-motivating team player with excellent interpersonal skills.
* Analytical and quality mindset with the ability to see the big picture without losing track of details.
* Empathic and adaptive personality.
* Excellent writing, presenting and negotiation skills.
* Proficient in English.

#LI-EUR

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com