Why Cmed? Cmed occupies a unique position in the clinical research industry, not only as an expert in the operational delivery of clinical trials for immuno-oncology and cell & gene therapies, but also as a developer of its own technologies for managing clinical data. This is a very exciting time to join Cmed, as we continue to leverage our considerable expertise in the delivery of clinical trials with our game-changing EDC and eSource platform, encapsia. Our unique combination of operational expertise and the latest technology helps reduce the costs and increase the speed of developing new medicines, essential to both improving and saving the lives of patients.
Cmed's Clinical Data Management Department is at the cutting edge, defining new and more efficient ways to design, capture, manage, review and visualize clinical trial data and we are now looking for a talented CDM Manager to join our team and help drive this change.
The RoleYou will provide leadership for clinical data management tasks and be responsible for the delivery of multiple, large or complex projects. Depending on your skills and experience, there may also be opportunities for line management responsibility, specializing in certain data management aspects and mentoring junior team members. This role can be remote anywhere in the UK or EU, or office based in West Sussex.
This role could be perfect for you if you:Have extensive clinical data management experience and a degree level qualification or equivalent experienceHave led multiple large or complex global oncology studies and study teams within a Contract Research Organization (CRO)Have hands-on experience in all end-to-end data management activities, including database design / UAT, third-party vendor management, (central) data review and close-outHave experience with defining data strategies and data flows for complex trials involving multiple data sources (incl. central lab, eCOA/ePRO, IxRS)Understand data structures e.g. CDISC CDASH and SDTMHave significant experience using reporting and data review tools and creating programming specificationsAre an excellent communicator and have experience working with global, cross functional teams and having direct client and vendor interactionsUnderstand medical terminology, clinical trial methodology and ICH/GCPHave proactively managed project budgets, timelines and resourcesHave experience with preparing and leading client meetings (e.g. proposal defence presentations, kick-off meetings)Are great at planning, well organised and can work calmly under pressureHaving been exposed to Central / Risk-based Monitoring and Real World Data is a plusWhat we offerA dynamic, friendly and supportive teamInnovative and exciting technologiesMentorship and training to further develop your skillsHome or office-based locationCompetitive compensation package
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