> Markdown version of [/jobs/ext/4083613-senior-central-data-monitor-all-genders](https://www.wearedevelopers.com/jobs/ext/4083613-senior-central-data-monitor-all-genders). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Senior Central Data Monitor (all genders) - **Company:** merck millipore - **Location:** UK - **Experience:** Expert - **Contract:** Permanent contract - **Skills:** Data Analysis, Clinical Data Management, Data Control, Data Integrity, Data Visualization, Monitoring of Systems, Microsoft Office - **Published:** October 1, 2026 - **Apply:** https://www.totaljobs.com/job/central-monitor/merck-millipore-job108211182 ## About the Role * Advanced degree in Life Sciences or a related field. * 7+ years of experience in central data monitoring, with some experience possibly gained in clinical data management, site monitoring, or risk-based quality management in clinical trials. * Strong knowledge of ICH GCP and regulatory requirements. * Proficient in data visualization and risk-based monitoring tools (e.g., CluePoints) and MS Office. * Excellent analytical and problem-solving skills. * Effective communicator with leadership capabilities. * Ability to manage multiple projects and priorities. * Detail-oriented and results-driven mindset. 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! ## Description As a Senior Manager in Central Data Monitoring (all genders), you will lead the identification and communication of risk signals in clinical studies. You will collaborate with cross-functional teams to ensure data integrity and support risk-based quality oversight. Your responsibilities will include supporting the development of applicable study plans, analyzing data trends, contributing to risk review meetings, and monitoring the implementation of corrective actions. Additionally, you will oversee quality checks to ensure compliance with industry regulations while driving continuous improvement in central data monitoring processes.