Location: Hamburg, Norderstedt - tesa HeadquarterEntry as: PermanentWork Area: Business Development, EngineeringWhat you will doAs part of our Smart Manufacturing organization, you will play a key role in enabling the reliable execution and scaling of customer
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 and
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, using
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 remote
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 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, including
Overview As Coherent Optical System Architect you will shape the next generation of coherent MODEMs on Nokia’s optical platform. You will work with prototype hardware and feedback loops to PIC and high-speed ASIC teams, driving performance