Medical Evidence Associate - Dermatology - VIE Contract

Medical Evidence Associate - Dermatology - VIE Contract

• Location: Netherlands, Amsterdam
• Target start date: 01/09/2025

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.

About the job

Looking to launch your career at the cutting edge of healthcare? Join Sanofi for a chance to develop with mentoring and guidance from inspirational leaders while helping to make an impact on the lives of countless people worldwide. As Medical Evidence Associate - Dermatology VIE in our Medical Evidence Generation Team for dupilumab in dermatology (atopic dermatitis, prurigo nodularis, chronic spontaneous urticaria, bullous pemphigoid,), you will work in close collaboration with seasoned medical professionals strategizing, leading, executing, and communicating on our extensive phase 4 study programme.

We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.

Main responsibilities:

• Strategically prioritizing medical data gaps within our global medical network.
• Developing innovative study protocols to address prioritized data needs.
• Executing phase 4 studies with operational excellence and adherence to budget.
• Building and maintaining industry-leading relationships with key opinion leaders, investigators, and other professionals involved in our study programs.
• Collaborating effectively with internal and external stakeholders to optimize cross-functional communication, enhance efficiency, and drive focused outcomes.
• Providing daily support to Medical Evidence Generation (MEG) team members to ensure smooth and efficient task completion.

About you

Experience:

• Experience in a similar field would be a plus.

Soft and Technical skills:

• Ability to evaluate and prioritize data gaps and align them with strategic goals.
• Skills in problem-solving to help design studies that address key data needs.
• Understanding of clinical study design, especially for phase 4 studies.
• Familiarity with medical data and the research process in a regulatory context.
• Basic project management skills to help plan, execute, and track study progress. Ability to work within budget constraints and timelines.
• Strong verbal and written communication skills for working with cross-functional teams, key opinion leaders, and other stakeholders.
• Skills in relationship-building to establish rapport with investigators and healthcare professionals.
• Ability to manage multiple tasks and maintain high standards in documentation and study protocol adherence. Detail-oriented approach to ensure accuracy in study execution.
• Ability to work collaboratively and supportively within the team. Adaptability to contribute to team goals and assist with daily tasks.
• Awareness of ethical, legal, and regulatory guidelines, particularly in phase 4 study execution.

Education:

• Bachelor’s or Master’s degree in Life Sciences (such as biology, biochemistry, pharmacology, or a related field).

Languages:

• Fluent English (written and verbal).