Amgen - United Kingdom

Senior EU Regulatory Affairs Manager sought to lead regional strategy and submissions for General Medicine at Amgen in Cambridge/Lisbon. Drive clinical trial and marketing applications, leveraging deep drug lifecycle knowledge and regulatory expertise. Requires a scientific degree, proven strateg...

Seeking a **Quality Compliance Senior Manager** to lead **Labelling & Regulatory Affairs** within R&D Quality. This Cambridge/Uxbridge role requires expertise in **GPvP**, **Regulatory Affairs**, and pharmaceutical quality management. You will drive compliance, manage audits, and oversee vendor q...

Amgen seeks an Observational Research Manager/Epidemiologist in Uxbridge, UK, to lead analyses on Real-World Data (RWD) assets. You will write Statistical Analysis Plans (SAPs), guide data analysts, and interpret study results using large databases like CPRD and HES. A Doctorate in Epidemiology o...

Lead clinical trial execution and strategy as a Director in the UK. You will oversee end-to-end site operations, ensure regulatory compliance, and develop high-performing teams. This role offers a chance to shape Amgen's portfolio with a focus on quality and patient safety, supported by a compreh...

Lead global value optimization and pricing strategy for a leading biopharmaceutical company. This senior role requires deep ex-U.S. market access expertise and experience managing international reference pricing risks. You will provide strategic guidance to senior leadership from a key UK locatio...

Lead global pricing strategy and risk management for a pharmaceutical portfolio in this key associate director role. Utilize advanced analytics to optimize launch sequences, manage international reference pricing, and ensure pricing governance. Based in the UK, this role offers significant career...

Lead global clinical programs, ensuring quality and efficiency in bringing innovative medicines to patients. This role requires strategic study design, risk management, and leadership of cross-functional and vendor teams across multiple geographies. Based in the UK, it offers vast career growth w...

Lead a global team in shaping patient-centric clinical trial consent. Drive the end-to-end development of compliant, high-quality Informed Consent Forms (ICFs) at scale. Leverage your life sciences expertise and vendor management skills in a strategic, cross-functional role. Enjoy career growth w...

Lead global clinical trial start-up as an Associate Director, managing a team to ensure speed, quality, and compliance. You will need a life sciences degree, project management expertise, and experience leading global teams. This role offers career growth, a comprehensive rewards package, and is ...

Lead the global Study Start-Up team to deliver high-quality clinical trials with speed and efficiency. This director role requires experience in clinical trial execution, managing global teams, and vendor oversight. Based in the UK, it offers a strategic leadership position with a focus on innova...