Company Description MSX International supports leading automotive brands worldwide, helping improve repair performance, customer satisfaction, and aftersales operations across 80+ countries. Job Description he Business Success Specialist is responsible for partnering with automotive workshops in our
#WeAreIn for jobs that impact everyones life. Optimize. Innovate. Deliver. Join us in redefining manufacturing excellence. As a (Senior) Supervisor Maintenance Automation on our Manufacturing and Operations team, find yourself in a high-tech world where silicon
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
Discover your exciting roleThe Expert Project Risk Management (m/f/d) ensures that project uncertainties are systematically identified, assessed, managed, and transparently reported, so that threats to project objectives are minimised and opportunities are actively exploited.The role supports
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
Description We are seeking a Environmental Compliance Manager to ensure environmental regulatory compliance across 15+ Amazon facilities in Germany, Poland, Czechia, and Slovakia. You will reduce compliance violations, implement risk mitigation programs, and serve as the
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
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
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 CRA role, you will monitor and oversee clinical studies at investigative sites to ensure quality and compliance with protocol, SOPs, ICH-GCP, and regulations. You will be involved in study setup, regulatory submissions, and
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 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 performance,
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 across
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 will own the proposal and deal management lifecycle for a leading international technology and consulting organization. You’ll coordinate cross-functional input to deliver high-quality, compliant, and competitive proposals on time. You’ll manage
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.
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 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