Global Clinical Development Strategy Expert
Sanofi

We are seeking a highly motivated medical doctor to join the Global Clinical Department team of Sanofi Vaccines. Within Sanofi Vaccines Research and Development, and more specifically the Global Clinical Development Department, and within the guidelines given by the Global Clinical Franchise Head, the Global Clinical Development Strategy Expert (GCDSE) is a key member of the Project Team and the Clinical Team.

The R&D project team, plans, develops and manages the project strategy, in order to obtain registration of a new product or improvement of a vaccine for the prevention and / or treatment of the disease. The GCDSE is responsible for the clinical development strategy and is a core member of the R&D Project team.

About the job

• The Clinical Team is responsible for the execution of the clinical development plan, specifically the clinical studies defined therein. The GCDSE leads the Clinical Team, ensuring that the clinical development strategy is executed according to the adequate processes and with the highest clinical and medical scrutiny.
• The candidate will report to the Global Clinical Franchise Head for Pneumo & New Targets and will be responsible for projects in the Pneumo Franchise.
• Intimately involved in clinical strategy, and all stages of operational clinical development.
• Define the strategic clinical development plan in line with the global R&D strategy, the specific Franchise (commercial) strategy and the Regulatory needs.
• Present, defend and get endorsement of the clinical strategic plan with the appropriate governance committees within Sanofi Pasteur.
• Support the different functions within the Clinical Team with his/her expertise and leadership (monitoring, data management, biostatistics, medical writing, pharmacovigilance, regulatory affairs) as well as interact with and support Project team members, Clinical Immunology Laboratory, Budget and Planning Functions, Legal and Patent Department, Product Brand Leader and Medical Affairs.
• Ensure that the operational development process is aligned with Sanofi Standard Operation Procedures (SOPs), and help to review and improve current SOPs.
• Manage the clinical development process from early stage development until licensure and provide clinical leadership for the generation of evidence from the clinical development data that will support the licensure and commercialization of the new vaccines (e.g. define evidence generation plan, lead interpretation of clinical data, provide decision-making pathways based on study outcomes, provide risk management analyses and mitigation plans etc) .
• Work closely with the pharmacovigilance department to define and ensure the process of safety surveillance during clinical development and design the safety risk management plan.

About you

• M.D. in a life-science area like Biology, Immunology, Pharmacology, etc. or a PhD with a minimum of 3 years' experience in Clinical Development.
• Expertise in immunology, specifically in the clinical development of preventive vaccinology is favorable with relevant experience or specialization in Infectious Diseases, Pediatrics, Internal Medicine or a background in clinical immunology is preferred
• Experience with working according to GCP/ICH guidelines
• Excellent interpersonal skills, experience with leading and managing transversal teams
• Take the lead for the preparation of key clinical documents to be prepared for clinical trials (protocols, reports), CTD submissions, interactions with Sanofi Pasteur governance bodies, external experts and committees.
• Build and maintain a strong network of internal and external collaborators, opinion leaders, investigators and competent authorities.
• Support the Global Clinical Development department with non-project related activities to continuously improve our way of working, and to maintain our position as center of clinical excellence for Sanofi and with external collaborators.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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