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Associate Director Clinical Data Manager (all genders)

Merck KGaA →Warszawa, Mazowieckie· posted Aug 24, 2026
Biostatistics / DataDirector

Exciting opportunity for an Associate Director Clinical Data Manager to lead and oversee clinical data management activities within our Data Monitoring, Management and Innovation department. Oversee the integrity and accuracy of clinical trial data, coordinate a team, and ensure quality deliverables. Ideal for experienced professionals in clinical data management with strong leadership and project management skills.

requirements

• Bachelor's or Master's degree in a scientific or technical discipline, preferably in life sciences, data management, or a related field • Minimum of 10 years of experience in clinical data management within the pharmaceutical, biotechnology, or healthcare industry • Profound, long-standing experience in leading clinical data management activities in complex Oncology development projects (including large phase III trials) both on trial and program level • Experience in working in different sourcing models with a focus on in-house models • Committed to continuous personal and professional development, and bringing external insights to the role to drive innovation and process improvement • Proficient in contributing to non-study related initiatives e.g. process improvements, in addition to study assignments • Strong project management, analytical, communication, collaboration, and problem-solving skills • Ability to work proactively and independently on assigned tasks or projects of varying complexity; prioritising and managing multiple activities simultaneously • Demonstrated ability to lead and oversee end-to-end data management activities within a clinical trial, as well as leading and coordinating global teams in a matrix organization • Familiar with autonomously providing reports to senior management, including updates on financials, forecasts and timelines • Proficiency in data management systems and tools, including strong knowledge of regulatory requirements, industry standards, and best practices related to clinical data management • Experience in Risk Based Data Monitoring/Management, and with clinical trial data standards, such as CDISC, is preferred 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!

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