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
Job DescriptionINTRODUCTION Do you get excited when guiding organizations on the transformation of their HR processes based on the next generation of technology? Put your expertise to work as part of the world’s largest independent technology
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
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.
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 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 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 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 lead transformation projects and strategic initiatives across mobility, automotive, and other sectors, shaping roadmaps and overseeing delivery. You partner with senior stakeholders to ensure high-quality outcomes, and you apply AI and
Overview In this role you lead international SAP S/4HANA Public Cloud rollout projects from initiation to go-live and stabilization. You collaborate with business and IT stakeholders to deliver scalable, standardized SAP solutions that create long-term value. You
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 in the Heidelberg/Stuttgart region, you will ensure site performance and data integrity across sponsor-led trials. You will work closely with site teams to maintain regulatory and GCP compliance, manage monitoring activities, and
Overview As a Workday Lead at Accenture, you drive end-to-end HR transformation using Workday within a global advisory team. You guide client workshops, lead workstreams, and ensure successful delivery of cloud-based HR solutions that align with
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