Deine Aufgaben 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. Dein Profil 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. Warum wir? 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 days per week in the office. Interessiert? We are looking forward to your application. Über uns We feel responsible. I n unserer mittelständischen und inhabergeführten CRO wiegt ein ehrliches und erfolgsorientiertes Miteinander stärker als eine fremdkapitalgesteuerte Firmen- und Personalpolitik. Wenn auch du Wert auf eine langfristig ausgelegte Zusammenarbeit in einem familiären Umfeld mit kollegialem, herzlichem und dennoch professionellem Arbeitsklima legst, dann bist du bei uns genau richtig.