Description Amazon Web Services (AWS) is looking to hire a highly motivated, customer-obsessed professional to provide hands-on support to our Data Center Infrastructure Operations team in Berlin. As a Data Center Security Manager (DSM), you will
Overview Senior Statistician at Viatris leads statistical design and strategy for clinical studies, ensuring high scientific and regulatory quality. You partner with clinical science, operations, regulatory teams, and CROs across multiple therapeutic areas. You drive methodological input, sample
Overview In this role you will craft country-specific compliance content that clarifies regulatory requirements for internal and external audiences. You will collaborate with global teams to ensure accuracy and alignment with Deel’s standards, while contributing to strategic,
Overview In this role, you will lead clinical trial operations for sponsor-specific partnerships in Germany, overseeing site and central monitoring with a focus on patient safety and data integrity. You will collaborate with cross-functional teams to
Overview In this role you lead Phase I clinical projects for a single sponsor, ensuring on-time study delivery within budget and regulatory guidelines. You act as the primary liaison between the sponsor and our company, coordinating cross-functional teams
Overview As a Senior Contract Associate, you drive the drafting, negotiation, and finalization of complex Clinical Site Contracts for clinical trials. You will serve as the liaison between CBO, GCO, Legal, sites, and external providers to
Overview In this role you will drive grid code compliance for renewable energy generation, supporting integration into power networks. You will work within a technical and certification-focused team to assess, model, simulate, and certify energy systems.
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 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 high-impact field role, you will serve as BeOne’s medical affairs representative to external medical communities, shaping scientific exchange and partnerships with HCPs and KOLs. You’ll translate complex data into actionable medical insights, support
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
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 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 In this Underwriter role, you will source and underwrite new Construction business to achieve profitability, building a robust, profitable portfolio. You will work within the Construction governance framework and coordinate with cross-functional teams to ensure
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 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 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