Overview In this role you support the JPMSE Recovery & Resolution agenda and act as the primary contact for senior management and regulators. You collaborate with Finance, Risk, Business Management, Treasury and Operations to coordinate plans, submissions
Job Description Summary As a Contract Manager for HVDC, you will play a pivotal role in delivering landmark projects that are central to Europes energy transition. Your contributions will be highly visible and instrumental in the
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 CRA for a single sponsor partnership in Germany, you will oversee site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. You will work with cross-functional teams to assess site
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 In this role you will support clinical trials in the Berlin/Leipzig/Dresden region, ensuring regulatory and protocol compliance across monitoring activities. You will work with site teams to safeguard data integrity, informed consent, and patient safety
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 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.
Overview As a Clinical Research Associate, you will oversee site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. You’ll work with cross-functional teams to protect patient safety and data integrity across trials,