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Medical Advisor - all genders

Berlin, Germany
Frankfurt am Main, Germany
Permanent Posted on   Feb. 26, 2025 Closing on   Mar. 16, 2025
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Medical Advisor - all genders

To ensure a rapid processing of your application, please apply only via the “Apply” button. Please include a letter of motivation and a current resume with your application.

About the job

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. Join our Clinical Study Unit (CSU)as Medical Advisor!

Medical Advisors provide medical and scientific expertise and guidance to investigators and CSU staff performing clinical trials within a CSU cluster to ensure patient safety and scientific integrity of the protocol which ensures the reliability of information provided to agencies at submission. They are therapeutically aligned medical experts in the country/region for the studies/projects they are responsible for.

Main responsibilities:

  • 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

About you

Education and qualifications:

  • Advanced university degree such as MD, PharmD, PhD in life science or equivalence. University degree in human medicine strongly preferred.

  • Solid knowledge of ICH, GCP and local regulations

  • Qualification in a medical specialization would be preferred but not required

  • Previous experience in Clinical Practice, Clinical Research and/or Drug Development is a plus

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.

Why choose us?

  • Bring the miracles of science to life alongside a supportive, future-focused team.

  • Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

  • Benefit from a well-thought-out benefits package that rewards your contribution and commitment.

  • We take care of you and your family with a wide range of health and social such as high-quality healthcare, numerous prevention programs and coverage for long-term illness. Our 14-week paid family leave for both parents is outstanding as well as a wide range of childcare benefits.

  • Start your career at an attractive location in the center or in the capital of Germany and experience our modern working environment and benefit from hybrid, flexible working time models.

Pursue Progress. Discover Extraordinary.

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. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.

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

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

#LI-onsite

#LI-hybrid

Pursue progress. Discover extraordinary.

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. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.

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

Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com

Apply Now
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