SOFT SKILLS:

• Excellent verbal and written communication skills to effectively interact with internal teams and external stakeholders.
• Strong analytical and problem-solving skills to address protocol-related questions and operational challenges.
• Leadership and Collaboration: Ability to lead and collaborate with cross-functional teams, including global R&D, pharmacovigilance, and regulatory affairs.
• Stakeholder Management: Proven ability to build and maintain relationships with investigators, trialists, medical experts, and Key Opinion Leaders (KOLs).

Languages:

• Business fluent in English and German, both written and verbal.

• Provide appropriate medical and scientific feedback to Local CSU operations teams as well as global R&D Medical Operations, i.e., Clinical Research Director (CRD), Global Feasibility Lead (GFL), TA early planning leads, global project team, pharmacovigilance, and regulatory affairs.
• Ensure the medical and scientific collaboration with medical functions in the respective Business Units in the countries of their responsibility and with investigators, trialists, medical experts, and Key Opinion Leaders (KOLs) in the country, region, or global level.
• Proactively assess opportunities to enhance sanofi’s medical/scientific value.
• Understand project needs and provide effective solutions when needed.
• Fosters relationships with internal and external stakeholders, even in complex environments.

Furthermore, the MDAs are responsible for:

• Providing local medical expert input into study design to help with the operationalization of studies
• Resolution of protocol related medical and scientific questions from sites
• MT trainings on the medical and scientific aspects of disease, compound, and protocol
• Country feasibility confirmation
• Setting of Diversity targets for assigned studies