Your mission You act as the primary point of contact for the study team and/or sponsor. You oversee study budgets and finances. You maintain study oversight through effective communication with key stakeholders. You develop appropriate study management plans. You manage project risks and resolve issues. You review monitoring visit reports. You maintain oversight of eTMF and ensure high quality. Your profile You have at least 4 years’ experience in clinical research and good knowledge of GCP. HRA/REC submissions in the UK are an advantage, however full training will be provided. You have a life science degree or healthcare equivalent (Bachelor). You have strong communication skills and fluency in English. You are proactive. You are flexible when the role requires. You are great at prioritising and problem solving. You are organised, punctual, have great interpersonal skills and happy to work with the team. You have an entitlement to work in the UK. You have a UK drivers licence. Why us? We ensure you a thorough introduction and support from a team of experienced natural scientists. We offer exciting and varied projects from the pharmaceutical, biotech and medical production sectors. We guarantee fast decision-making processes due to flat hierarchies and “open doors” culture. We love diversity! Our teams are diverse, cross-generational and we work and learn with and from each other. We have modern, well-equipped offices. We provide flexible home office options with a minimum of 2-3 days per week in the office. Interested? We are looking forward to your application. About us We feel responsible. In our medium-sized and owner-managed CRO, honest and success-oriented cooperation is even more important than a company and personnel policy controlled by external capital. If you also value long-term teamwork in a family environment with a collegial, cordial and yet professional working atmosphere, then you have come to the right place.