Operational Data Steward Leader
布达佩斯, 匈牙利 Permanent 发布于 Apr. 02, 2026 申请截止于 Apr. 21, 2026- Job title: Operational Data Steward Leader
- Location: Budapest, Hungary
- Job type: Permanent, full-time
- Hybrid working
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.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Join our global Data Intelligence for Clinical Operations (DICO) team as an Operational Data Steward Leader and you’ll be accountable for the strategy and coordination of the E2E governance of clinical operational data: study design characteristics, study stakeholders (study team members, vendors, investigational sites, HCPs…), study milestones and status, study recruitment data. You’ll also present this strategy to Top Management via the DICO Steering Committee.
Be part of something exceptional. Our Budapest Hub has been recognized for workplace excellence, innovation, and our commitment to putting people first. See the full list of our awards at the end of this posting.
Main responsibilities:
1. Liaise with study teams - Study support for operational data
• Serve as Strategic primary contact for end-users within Clinical Operations answering to any questions, requests from other functions. Coordinate the requests review management of study-specific operational data at study level and / or updates in dictionaries in master data systems, based on customer needs. Understand business needs of study end-users, define or update operational data and associated process and quality rules.
• Coordination of transversal groups to manage Use Cases to align operational players for agile/fast decision making and delivery of common operational deliverables. Ensure cross-functional vetting and awareness of implementation activities across Therapeutic Areas.
• Lead the implementation of the effective solution in addressing quality and consistency measures depending on data criticality, including definition harmonization, investigations and impact analysis for functions using these data.
2. Clinical Operations Data Foundations
• Lead the management of Operational Data Standardization (definition, dictionaries, data flow to consuming systems…) in using common vocabulary for a same concept used by several functions. Supervise the reference data development and cleaning in a harmonized way in systems.
• Drive policy-related actions: Streamline processes and associated quality documents (global SOPs, policies, guidelines…) that describe the management of the operational data and implement new working practices. Define the level of control based on data criticality (ex: Reg transparency… vs internal).
• Recommend data flow optimization, capitalizing on electronic tools, to address new requests and assess their impacts to shorten the cycle time and improve overall quality. Manage regular analysis of information reported from a broad variety of sources. Lead the digital transformation to implement an automatic process (AI, ML, NLP…) linked to the operational data to propose data related evolutions.
• Define and coordinate the monitoring of data governance processes adherence to target model and good use of data in clinical trials managed by Clinical operations (KPI or data quality metrics and deviations from acceptable levels).
3. Train and communicate
Support the DICO Head in change management activities to drive a data-driven R&D organization:
• Drive supporting documents for communication, education and trainings related to Operational Data assets
• Organize communications on updates or evolutions, users feedback, exchange of best practices and lessons learned. Promote operational data activities (including new usages)
About you
Experience:
- At least 5 years in Clinical Development with background in clinical study management. Background or great interest in databases management.
Soft Skills:
• Good communication skills and ability to facilitate common understanding of people with various backgrounds, collaborative spirit
• Strong organizational skills, efficiency in matrix organization. Ability to effectively handle multiple tasks and to prioritize, results oriented
• High level of autonomy and commitment
• Customers & quality focused. Ability to simplify complex processes in developing guidelines and tools
• Flexible and Open-minded, Eager to learn with interest and ability to understand new perimeters
• Problem-solving and decision-making capabilities, with analytical and synthetic spirit.
• Project management skills: able to monitor a process, and lead to progress and results. Ability to anticipate, timely escalate issues and define appropriate action plans.
• Good Knowledge and familiarity with industry standards and practices, clinical development process, international regulatory guidelines and GCP requirements
• Good English Communication level (written and oral)
Technical skills:
• Excellent transversal understanding of the Data Flow and Data Management processes in Clinical Development.
• Experienced with clinical data management systems and has a sound understanding of database and programming concepts, database structures, file structures (CTMS and satellites, planning tools…)
• Interest for technical evolutions – Digital-oriented. Up to date knowledge on clinical governance systems such as MDM, Data Catalog and data mapping solutions
Education:
PharmD or Master’s degree in relevant scientific and/or medical field
Language(s):
- Strong English skills (verbal and written), ability to exchange fluently in a global environment
Why choose us?
- Bring the miracles of science to life alongside a supportive, future-focused team in an international work environment
- Work from an "Office of the Year 2025" award winner with flexible home office policy
- Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact
- Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave
- An individual and well-structured introduction and training of new employees and we will dedicate a Buddy for you to better navigate in your first weeks
- Join a great community & special events (Monthly Board Game Nights, Summer Events, Well-Being Lectures & Sport Clubs)
Office of the Year 2025 – Evolution Award
Our most recent award – Sanofi is recognized for creating an innovative workspace that supports collaboration and adaptability.
Marketing Diamond Award 2026 – Employer Branding
One of the highest honours at Hungary's prestigious Marketing Diamond Awards, recognizing excellence in employer branding.
BSC Investor of the Year 2025
Awarded by HIPA, ABSL Hungary, and AmCham Hungary for our contribution to Hungary's business services sector.
PwC Workforce Preference Survey 2025 – Top 3 Most Attractive Employers
Ranked 3rd among the most attractive employers in Hungary.
Hungarian Employer Branding Awards 2025 – Gold & Silver
Best Strategic Employer Branding Campaign (Gold) and Best Employer Branding Campaign in the Pharma Sector (Silver).
PursueProgress. 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!
Discover our Code of Conduct, that serves as the moral compass that guides us when chasing the miracles of science to improve people’s lives. Please ensure to have read this document before applying.
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null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!
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。
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