Work ScheduleOther Environmental ConditionsOffice Job Description About Us At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Our Mission is to enable our customers to make the world
TYTAN Technologies The PACE is fast. The expectations are high. The contribution matters. Working at TYTAN is more than a job, this is a mission. We thrive, think big, and hold ourselves to the highest standard.
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description About Us At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Our Mission is to enable our customers to make the
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description About Us At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Our Mission is to enable our customers to make the
Remote Frankfurt Stuttgart - MSO Remote Germany Munich Dusseldorf - MSO Berlin - MSO Full time R- Job summary The Red Hat Sales team is seeking a Specialist Solutions Architect to join us in Germany. In
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description About Us At Thermo Fisher Scientific, youll discover meaningful work that makes a positive impact on a global scale. Our Mission is to enable our customers to
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description About Us At Thermo Fisher Scientific, youll discover meaningful work that makes a positive impact on a global scale. Our Mission is to enable our customers to
Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is
Job summaryThe Red Hat Sales team is seeking a Specialist Solutions Architect to join us in Germany. In this role, you will support the Ansible Sales team and provide pre-sales technical support to prospects. Youll work
Are you a structured and experienced Technical Project Manager (m/f/d) with a passion for hardware development? Are you eager to take ownership, drive cross-functional collaboration, and lead projects from idea to mass production? Then join our
Overview In this role you will monitor clinical studies at investigative sites and ensure compliant conduct, data integrity, and study reporting. You will set up and oversee study activities, including site identification, regulatory submissions, and initiation visits. Working in
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 and
Frankfurt / Berlin / Cologne / Dusseldorf / Hamburg / Munich / StuttgartClinical Services – Clinical Study Delivery - Monitoring & Site Management /Full-time, Permanent /RemoteResponsible for the clinical operations of a project within a defined regional/global
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 a collaborative team.
Overview In this role you coordinate investigator grants and contracting activities to support proposal development and trial initiation. You will maintain contracting systems, produce specialist contract language, and align with sponsor requirements and RSU plans. You’ll collaborate
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, collaborating with cross-functional
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 real-world
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 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 remote
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 project teams