Job SummaryOur clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team in Munich. This position plays a key role in the clinical
Job descriptions may display in multiple languages based on your language selection.What we offer:At Magna, you can expect an engaging and dynamic environment where you can help to develop industry-leading automotive technologies. We invest in our
About LucidAt Lucid, we are creating exceptional mobility experiences through innovation to drive the world forward. Built on Lucid’s proprietary technology and software-defined vehicle architecture, our award-winning vehicles bring our “Compromise Nothing” approach to the global
GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver 40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the
DescriptionDirector of Product Management Hybrid (minimum of 2-3 days a week from the office)Shape the Future of PrivacyUsercentrics is a global leader in data privacy and privacy-led marketing solutions. We believe there is no need for
Marketing teams are stuck between fragmented customer data and martech stacks that copy that data into proprietary silos while customers expect real-time, personalized experiences. Customer Lake, the agentic Customer Data Platform (CDP) built natively into Databricks,
Overview As a Clinical Research Associate in Real World Late Phase, you monitor and manage trial sites to ensure regulatory compliance and data integrity. You will perform remote and on-site activities across initiation, monitoring, and close-out,
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 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 II for our multisponsor team in Germany, you oversee site performance and trial data integrity through monitoring and site management. You align with ICH-GCP, GPP and protocol requirements, liaising with site staff
Overview In this role you will lead global start-up activities and ensure compliant, timely submissions within our clinical operations team in Munich. You will liaise with cross-functional teams to manage submission documents, informed consent, and regulatory reviews, shaping
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 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, 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,