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CSU Regional Quality Lead, Process & Training
多个地点 Permanent Posted on Feb. 12, 2025 Closing on Mar. 05, 2025CSU Regional Quality Lead, Process & Training
- Location:Hungary, Budapest or Belgium, Diegem or Czech Republic, Praha or Denmark, Berlin, or Italy, Milano or Poland, Warsaw
- Hybrid working pattern
About the job
This position is open to all countries with a CSU Footprint in EU.
The CSU Regional Quality Lead Process and Training (RQLPT) is a Clinical Study Unit (CSU) region-based role which is part of a broader network of quality professionals who ensure alignment and compliance to the Sanofi R&D quality system and related clinical operations activities within the Sanofi Group and are linked to Clinical Sciences & Operations (CSO) Platform. This role also works in collaboration with the respective Country Quality Head (CQH) at country level(s) to ensure local clinical studies related activities are managed as per the expectations within the Global Quality System and R&D Platform and other local GXP related activities.
As such, the Regional Quality Lead Process and Training acts as an extension of the Clinical Quality & Continuous Improvement department (CQ&CI) at regional level (CSU and satellite related countries) for the management of Quality Documents / Processes and for any action toward the continuous improvement and optimization of these.
The Regional Quality Lead Process and Training is responsible to develop, monitor and adjust the End-to-End Quality Document (QD) strategy for the CSU worldwide together with the CSU Quality leads Process and Training from the other regions and the Head Global CSU Process and Training. They ensure the identification, development, support, implementation and improvement of clinical global and local CSU QDs. They assess and decide on the need for local CSU QDs and process manuals in collaboration with the Head global CSU Process and Training and the CQ&I representative for this topic.
The Regional Quality Lead Process and Training develops, oversees, and ensures updates and governance, of the training program. They identify needs for training and prepare/update/review any of CSU-related training program topics [e.g. for new global and local tools, other local requirements and /or specificities).
The Regional Quality Lead Process and Training is in charge of overseeing and promoting the maintenance of the appropriate qualification of the CSU staff and the documentation thereof for:
- Corporate & CSU country/cluster (local) QDs and process manuals.
- Good Clinical Practices (GCP).
- International and local regulations.
- Study management activities (e.g. mandatory role-based training).
- Corrective & Preventive Actions (CAPA) in case of signal detection.
- Collaboration with partner(s) to deliver CSU‐specific training.
About you
- In-depth knowledge of ICH-GCP, regulatory, and ethical frameworks for clinical studies.
- Level 3 Risk Management: Anticipate, adapt, and execute plans to manage risks and foster innovation, while protecting company assets (Sanofi First).
- Level 2 Project Management: Strong organizational skills for managing multiple projects and stakeholder engagement.
- Level 3 Data Analytics: Analyze data trends, predict, forecast, and use benchmarks for strategic decision-making.
- Level 1 Medical/Scientific Knowledge: Understanding of R&D therapeutic areas.
- Level 3 Clinical Development Knowledge: Understands governance, product life cycle, and supports internal stakeholders (e.g., GBU, PV, Regulatory).
- Level 3 Problem-Solving: Apply critical thinking, measure outcomes, and implement solutions.
- Level 2-3 Business Acumen: Understands operations, departmental synergies, and aligns with strategic goals (internal and external).
- Level 3 Change Management: Support change, overcome resistance, and act as a change agent.
- Level 3 Emotional Intelligence: Integrate emotional awareness and social skills to manage relationships effectively.
- Level 3 Interpersonal & Relationship Management: Influence and inspire others while respecting their opinions.
- Level 1 People Development: Demonstrates essential people management qualities, such as setting SMART goals and performance discussions.
- Trained in Compliance and Business Integrity.
- Strong presentation, coaching, and mentoring skills.
- Excellent communication and negotiation skills across global teams.
- Proficient in IT tools (e.g., MS Office) for training materials and tracking.
- Fluency in English (oral and written).
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.
#LI-EUR
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!
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共享中心
从波哥大到布达佩斯,从吉隆坡到海得拉巴,我们的版图上处处都有您的全力付出。如果您选择在共享中心施展抱负,您将身处全球变革的中心。我们无惧艰难,并肩作战,努力缩短新药抵达患者手中的时间。您将充分发挥创造力,成就独一无二的自我,从而帮助其他人拥有健康生活。让我们努力探索先进科技,改变更多人的生活。
体验可能性
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我们的办公地点
我们的员工遍布60多个国家/地区。他们勠力同心,携手共创医疗健康领域的美好未来。无论您在哪里工作,我们的专家都会指导您推动职业发展,您也将能够运用先进的科学技术,取得意义非凡的重大突破。
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勇敢追梦,奔赴美好未来
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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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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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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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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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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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。
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