P95 Julius Clinical has become AKEURA, a specialist contract research organization (CRO) helping sponsors advance medicines across their full lifecycle. Our dual expertise in early- through late-phase clinical development and real-world evidence is delivered by hands-on clinicians, scientists, and epidemiologists, drawing on more than 25 years of experience. We’re built on the belief that a team of the right people, giving everything they’ve got to the needs of the study, will outperform any other approach. Our team of more than 500 experts spanning five continents has delivered more than 1,000 studies in over 75 countries, including regions where patients are hardest to reach. AKEURA exclusively focuses on three therapeutic areas: neuroscience, infectious diseases and vaccines, and cardiometabolic diseases. Across each, we bring the experience, reach and hands-on expertise to give every promising medicine the study it deserves. • Provide leadership of one or more complex metabolic continuum projects in the delivery of services and key milestones to make sure that projects are delivered according to the client expectations and project scope, time schedules and budget • Develop study-specific documentation in collaboration with compliance and study teams • Monitor progress against plans, KPIs, and budgets; adjust as needed • Identify and mitigate risks proactively • Report progress to sponsors, internal stakeholders, and steering committees • Act as the day-to-day contact for sponsors and project teams • Drive process improvements and contribute to departmental growth • Manage project finances and support proposals and bid defense meetings • Resolve complex challenges through effective stakeholder engagement • Participate in and support commercial-team led activities such as project strategy development, proposal development, BDM and client meetings. As a (Sr) Clinical Project Manager in our cardiometabolic business unit focusing primarily on metabolic continuum studies, you will lead complex, sometimes global, clinical trials from start-up to close-out, ensuring delivery within scope, budget, and timelines. You will manage multidisciplinary teams, act as the primary contact and partner for sponsors, drive excellence in compliance with ICH-GCP, protocols, and SOPs • Minimum 10 years’ experience in clinical trials (pharma and/or CRO), with at least 5 years as Project Manager • Extensive metabolic continuum study experience including but not limited to obesity, diabetes, MASH, dyslipidaemia, ASCVD, is required • Proven ability to create strong relationships with small sponsor stakeholders including CEOs • Multinational study experience • Outstanding presentation skills • Advanced business acumen and using data to influence decision makers • Strong knowledge of ICH-GCP and relevant regulations