Senior Clinical Data Manager (all genders)

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

A great opportunity has opened within the Data Monitoring, Management and Innovation department to further strengthen our Clinical Data Management team.  As a Senior Clinical Data Manager, you will play a crucial role in managing and overseeing clinical data management activities within the organization. You will be responsible for ensuring the integrity, accuracy, and completeness of clinical trial data, while also coordinating a team of clinical data management professionals in a matrix setting.

This role requires to be on-site in our office in Warsaw, Poland for 3 days per week.

Your role: As a Senior Clinical Data Manager (all genders), you will be accountable for the delivery, quality, integrity, and submission-readiness of clinical trial data for assigned global Phase I–IV studies. In this role, you will implement risk-based data collection, cleaning, review, reconciliation, and quality activities across electronic data capture (EDC) and external data sources, while representing Clinical Data Management on the Core Trial Team for assigned studies.

You will lead the project management of all study-level data management deliverables, including timeline planning, resource coordination, risk identification, issue resolution, and stakeholder communication across internal and external partners. You will oversee day-to-day CRO/vendor activities, support compliance with regulatory requirements and industry standards such as CDISC, and help ensure that clinical data packages are complete, accurate, and submission ready. Beyond study execution, you will contribute to the evolution of data management standards, SOPs, best practices, and process improvements, including the effective use of automation, advanced analytics, and AI-enabled solutions where appropriate, while sharing knowledge and supporting the development of colleagues within Clinical Data Management.

Who you are:

You hold a Bachelor's or Master's degree in a scientific or technical discipline, preferably in life sciences, data management, or a related field

You have a minimum of 8 years of experience in clinical data management within the pharmaceutical, biotechnology, or healthcare industry, with a demonstrated track record of delivering end-to-end data management activities for global clinical trials

You bring strong project management, communication, collaboration, and problem-solving skills, with the ability to work independently and proactively on studies and projects of varying complexity

You have experience coordinating global, cross-functional teams in a matrix organization, including managing day-to-day CRO/vendor activities and resolving operational issues

You are proficient in clinical data management systems and tools, with sound knowledge of regulatory requirements, industry standards, and good practices in clinical data management

You have experience with clinical trial data standards, including CDISC, and understand the requirements for complete, accurate, and submission-ready clinical data packages

You are committed to continuous personal and professional development and bring relevant external insights to support innovation, process improvement, and the effective implementation of data management standards and processes

Experience with Risk Based Data Monitoring and Management is preferred.  Experience using or supporting the implementation of automation, advanced analytics, and/or AI-enabled solutions in clinical data management is an advantage

Your main benefits:

Health and well-being: Get access to private medical care, life insurance, and sports card, receive prepaid lunch card

Work-Life balance: Enjoy additional paid days off, flexible working hours

Learning and Development: Take advantage of co-financing for language courses, trainings, and certifications as well as other development opportunities

Employee support and engagement: Benefit from Employee Assistance Program and join employee engagement groups for support and connection

Information on how we process your personal data for recruitment purposes, you can find on the registration form in our Recruitment Portal

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!