Overview As Clinical Development Lead for CRM, you will own the strategic and operational direction of the clinical development plan for this asset in Germany. You will guide a team of clinical leaders to execute a data-driven program aligned with the
Overview As Senior Clinical Program Lead, you will drive phase II–III development for obesity and liver diseases within a newly formed Global Clinical Development group. You will steer cross-functional teams to deliver high-quality trial execution and shape regulatory and medical
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
Overview As Senior Manager, Clinical Operations, you will lead governance and continuous improvement of clinical operations processes across regions. You’ll own the lifecycle of SOPs, work instructions, and templates, ensuring compliant, scalable practices. You’ll partner across functions to
Overview In this role you will provide on-site clinical support during interventional vascular procedures, work with physicians to optimize therapy and deliver trainings. You will lead market-facing activities in the region, collaborating with cross-functional teams to drive
Overview In dieser Rolle gestalten Sie maßgeblich die Positionierung und das Wachstum eines strategisch relevanten Therapiefeldes Neuromodulation in Deutschland und Österreich. Sie arbeiten eng mit Sales, Marketing, Market Access, Clinical und externen Partnern zusammen, um Adoption und
Overview In this role you lead trial monitoring staff (CRAs) within the country to ensure high-quality clinical trial execution. You work closely with the Regional Clinical Operations Manager to meet study timelines and quality standards, while supporting start-up
Overview In dieser Rolle steuern Sie die Umsetzung der kommerziellen Cardiac Solutions-Strategie in Europa und treiben nachhaltiges Wachstum durch innovative Geschäftsmodelle und strategische Partnerschaften. Sie arbeiten eng mit dem IGTD Europe Leadership Team zusammen, um die
Overview As Senior Manager, Clinical Operations, you will lead governance and continuous improvement of Clinical Operations processes across regions. You will own SOPs, templates, and process documentation, ensuring compliance and scalable workflows. You will collaborate with QA, Regulatory,
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 In this role, you drive early-phase obesity and liver programs from strategy through execution, leading cross-functional teams to advance therapies. You’ll influence regulatory strategy and contribute to Medical Affairs plans, shaping evidence generation and decision-making
Overview In this role you will spearhead clinical education and hands-on training for wound care solutions across North Germany, supporting sales and clinical services. You’ll work closely with the Regional Business Manager to drive product adoption, elevate customer
Overview In this role you drive the design and execution of early-stage oncology clinical development plans, leading cross-functional teams to translate strategy into patient-ready programs. You will shape trials, contribute to regulatory and Medical Affairs strategies, and evaluate
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 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 As a Project Manager in Medical Writing, you lead and develop a capable team to deliver compliant, high-quality medical writing outputs within sponsor partnerships. You align with clinical development objectives and collaborate across functions to shape document
Overview As a (Senior) Associate Director / (Senior) Patient Safety Physician, you will lead or contribute to global pharmacovigilance and risk management for compounds in development or on the market. You work cross-functionally with Clinical Development and Global Patient
Overview In this role you ensure scientifically sound, compliant clinical documentation to support development, approval, and commercialization of medical devices. You partner with cross-functional teams to address scientific and regulatory questions, improving product documentation, regulatory submissions, and post-market
Overview In this role you will drive awareness, access, and support for patients with rare liver diseases in Germany. You will develop and execute strategic account plans, partnering with healthcare professionals and multidisciplinary teams to identify
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