In this role, you will run quality management related projects with strong focus on digitalization. You translate regulatory and operational QM requirements into scalable solutions, ensure process robustness and data integrity, and lead cross‑functional roll‑outs from concept to
Rostock, Mecklenburg West Pomerania, Germany Full time R IQVIA - The Human Data Science Company - ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und
Overview In this role, you will serve as Germany’s primary compliance advisor, guiding the local business within BioMarin’s global compliance programme. You will lead risk assessment and mitigation efforts, partner with cross-functional teams, and drive regional
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 manage risks,
Overview As the regional trade compliance expert for EU/UK/CH, you manage import/export compliance, licensing, classifications, and sanctions, collaborating with brokers and authorities. You will monitor regulatory changes, develop controls, and support audits while ensuring seamless cross-border
Overview In this ORSA role, you apply quantitative methods to support national security missions from Stuttgart, delivering advisory, training, and operational support across commands. You will build and validate analytical models, synthesize findings for decision-makers, and
Overview In this role you will lead the monthly and quarterly close and own the validation of financial data from Deel’s internal finance integrations. You will design and QA accounting figures, ensure US GAAP compliance, and partner
Overview In this role you will define and govern the security architecture for Helsing’s CA-1 platform, spanning hardware and software design to regulatory compliance. You will craft the aircraft-level security concept, manage intra- and inter-vehicle communications
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
Overview As a Process Architect, you will lead the shift from document-centric to data-centric validation within Veeva Validation Management. You’ll translate legacy processes into normalized data ecosystems and guide customers through digitalization of validation workflows. This role combines
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 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
Overview In this role you will drive growth in Germany’s military sector by selling integrated defense solutions for land and naval applications. You will work with strategic defense stakeholders, co-developing tailored architectures and managing full sales
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 study
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
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
Overview In this role you will support enterprise IT operations in a secure environment, providing on-site end-user support and maintaining infrastructure. You will work across multiple locations in Europe and the Middle East to keep systems
Overview In this role you will ensure production uptime and service levels for Oracle Cloud environments across OCI and ERP systems. You’ll drive stability, performance, backup, recovery, and security, including orchestrating upgrade cycles. You will partner
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
Overview In this hybrid role, you will blend hands-on software development with systems integration and business automation to support USAFRICOM’s mission. You’ll work on enterprise solutions using Power Platform and ServiceNow, shaping data flows and AI-enabled workflows.