Senior Clinical Data Manager (all genders)
About this opportunity
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:
Bachelor's or Master's degree in a scientific or technical discipline, preferably in life sciences, data management, or a related field
Min. 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
Strong project management, communication, collaboration, and problem-solving skills, with the ability to work independently and proactively on studies and projects of varying complexity
Experience coordinating global, cross-functional teams in a matrix organization, including managing day-to-day CRO/vendor activities and resolving operational issues
Proficient in clinical data management systems and tools, with sound knowledge of regulatory requirements, industry standards, and good practices in clinical data management
Experience with clinical trial data standards, including CDISC, and understand the requirements for complete, accurate, and submission-ready clinical data packages
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
Job details
How this role compares
Computed from every other active Clinical Development role in our database, not just this employer's listings.
We currently track 307 comparable Manager Clinical Development roles across 69 biopharma companies.
Salary context
78 of 307 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 307 comparable roles
+ 20 more countries
Seniority mix
307 of 307 peers have a known seniority level
Therapeutic area mix
30 of 307 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
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How we calculate "similar"
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.