
Head of Biospecimen Management - all genders
法兰克福, 德国蒙彼利埃, 法国
塞纳河畔维提, 法国 Permanent 发布于 Sep. 12, 2025 申请截止于 Oct. 15, 2025
About Sanofi:
We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
About the Job
Biospecimen Management is a global team and, within the Translational Medicine Unit, part of Operations. The team is responsible for sample collection, handling, and logistics of samples that are collected for pharmacokinetic, immunogenicity, or biomarker analyses in Sanofi's clinical trials.
Main Responsibilities:
- Leads a global team that supports all aspects of sample management for clinical trials of all phases.
- Supports some aspects of the management of pre-clinical biospecimens.
- Responsible for the strategy of Biospecimen Management for biomarkers and bioanalysis.
- Oversees the activities of the biospecimen management team:
- Implementing the translational medicine strategy (e.g., Biomarker/Companion Diagnostics, pharmacokinetic, anti-drug antibodies) of clinical trials, focusing on biospecimen operations.
- Reviewing clinical trial protocols and Informed Consent Forms to ensure that the collection and analysis of biological samples are conducted according to the protocol and the biomarker plan, and in alignment with regulatory guidance.
- Preparation of study-related documents, e.g. Study Sample Management Plan.
- The entire business process of biospecimen lifecycle, ensuring that samples are collected, shipped, processed, analysed, and stored with the highest degree of quality and in compliance with applicable regulations.
- Tracking and managing all sample related activities for PK, PD, and biomarkers; supporting discrepancy resolution between CL and BA laboratory.
- Setting up the analytical Laboratory Information Management System software to register biospecimen of clinical trials to be prepared for analysis.
- Registering of samples, label preparation, correct storage, and compliant destruction.
- Accountable for quality and compliance in the handling of clinical samples; assures accuracy of sample delivery for analysis.
- Supports the management of 'precious' samples and samples for future use.
- Works with local teams to manage clinical samples according to health authority guidelines and quality requirements defined in GLP/GCP.
- Liaises with the clinical study organisation, bioanalytical experts, and external partners (e.g., CRO, analytical labs) to ensure cross-functional alignment, and adherence to deliverables and timelines.
- Devolops productive working relationships with central labs, ensuring the shipping, delivery, and quality of biospecimen fulfil Sanofi expectations.
About you
Experience:
- Master's Degree in a biomedigal or related discipliine and 5 years + of leadership experience in a pharmaceutical environment
- Practical experience in sample management
- Operational experience in clinical studies
- At least 8 years in a pharmaceutical environment
- Project management experience
Soft skills:
- Excellent communication skills
- Mind set for high quality
- Respectful of timelines
- Collaborative team worker
Technical skills:
- Familiar with requirements of regulatory authorities (GCP, GCLP, international guidance)
- Solid understanding of the operational aspects of clinical trials
- Knowledge of biomarkers, PK, ADA, and bioanalysis.
Education:
- Degree in a biomedical science or related discipline
Languages:
- English fluent, French and German a plus
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.
PursueProgress. Discover Extraordinary.
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and 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, gender identity, protected veteran status or other characteristics protected by law. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
#LI-Hybrid
#Biomarkers
#ClinicalStudies
追寻 发展。探索 菲凡。
进步需要我们每个人的参与——不论其背景、地域、或职业,我们都有一个共同的愿望:创造奇迹。你也可以成为其中的一员。我们不断追求变革,拥抱新思想,探索我们所能提供的一切机会。让我们一起追求进步。共同发现非凡。
在赛诺菲,不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同,我们为所有人提供平等的机会。
观看 “在赛诺菲的一天” ,并在官网 (sanofi.com) 上查看赛诺菲的多元化、公平与包容倡议!

在法国的职位
我们在法国拥有20,000名员工,分布在28处办公地点。他们肩负着相同的使命:将药物和疫苗带给最需要的人。从入职第一天起,您就能参与重要项目,找到职业发展的航向。无论您是研究员还是市场营销人员,我们都将为您提供相应的工具、资源和支持,帮助您不断追求进步。发展您的个人能力,携手具有包容性的团队,一起改变全球数百万人的生活。
体验可能性
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我们的故事
我们关注每一个员工的声音。因为,我们的未来取决于所有员工的付出与努力。正因为他们的助力,我们才能追求远大的理想。
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心怀梦想,成就一番事业
我们希望您以饱满的热情投入到自己的工作岗位中,给全球数百万人带来美好生活。您的职业发展道路由您自己来掌控。您只管制定目标,我们会提供充足的培训机会和支持,让您得偿所愿。
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想要改变自己的生活,乃至改变全球数百万人的生活,该怎么做?加入我们,开启职业新篇章,然后在我们的保驾护航中展翅高飞,并向优秀的人求教,为这份事业做出切实的贡献。
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我们的人与文化
我们是首个建立多元化、公平性和包容性(DE&I)委员会的制药企业。我们还建立了“菲常联盟”,为每位员工提供发声的平台。您的声音是我们建设未来道路的重要基石。
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您和我们相互依存,共同成长
我们精心打造薪酬体系,为您的身心健康、财务健康与社交健康提供全面保障。我们有着海纳百川的包容性团队文化,无论您在哪个岗位,都能展翅高飞。
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为什么选择我们?
我们为您提供各种工具、支持和培训机会,帮助您实现自己的目标。我们也希望您充分发挥潜力,帮助我们实现目标:将新药研发到临床治疗的时间减半。