Overview In this role you will develop, monitor, and report construction schedules for retrofit and upgrade projects in data centres across Europe. You will liaise between planning and delivery teams to ensure schedules align with SOPs, drive
Overview In this role you lead Phase I clinical projects for a single sponsor, ensuring on-time study delivery within budget and regulatory guidelines. You act as the primary liaison between the sponsor and our company, coordinating
Overview In this role, you will lead clinical trial operations for sponsor-specific partnerships in Germany, overseeing site and central monitoring with a focus on patient safety and data integrity. You will collaborate with cross-functional teams to
Overview In this role you lead trial monitoring staff (CRAs) within the country to ensure high-quality clinical trial execution. You work closely with the Regional Clinical Operations Manager to meet study timelines and quality standards, while
Overview In this role you support clinical trial sites to ensure regulatory and protocol compliance across a multi-sponsor program. You work with cross-functional teams to monitor data integrity, manage site activities, and drive quality through both
Overview In this PV Systems and Data Analysis role, you ensure compliance with PV SOPs and health authority regulations while supporting system administration, validation, and data retrieval. You will collaborate with global PV users, guiding them through
Overview In this role, you will monitor clinical sites to ensure regulatory and protocol adherence, overseeing data integrity and patient safety. You will collaborate with cross-functional teams across Austria and Germany, applying GCP/ICh guidance and SOPs. You’ll
Overview As Senior Manager, Clinical Operations, you will lead governance and continuous improvement of Clinical Operations processes across regions. You will own SOPs, templates, and process documentation, ensuring compliance and scalable workflows. You will collaborate with QA,
Overview As Senior Manager, Clinical Operations, you will lead governance and continuous improvement of clinical operations processes across regions. You’ll own the lifecycle of SOPs, work instructions, and templates, ensuring compliant, scalable practices. You’ll partner across functions
Overview As a CRA at Allucent, you monitor investigational sites, ensure trial integrity and patient safety, and drive compliant study execution. You will own site relationships and serve as the bridge between sponsor and site within
Overview As a Clinical Research Associate, you oversee site qualification, initiation, monitoring, and close-out to ensure protocol and regulatory compliance across Germany. You work with cross-functional teams to safeguard data integrity, patient safety, and trial quality,
Overview As a Clinical Research Associate with Syneos Health in Germany, you will oversee site qualification, initiation, monitoring, and close-out to ensure regulatory and protocol compliance. You’ll assess site performance, support data integrity, and manage communications
Overview As a Project Manager in Medical Writing, you lead and develop a capable team to deliver compliant, high-quality medical writing outputs within sponsor partnerships. You align with clinical development objectives and collaborate across functions to shape