About the RoleLeads and evaluates medac’s Managed Access Programs (MAP) and Named Patient Use (NPU) requests from a clinical and ethical perspective, ensuring robust benefit–risk assessments and patient-focused decision-making.Hands-on Medical Expert responsible for executing clinical-scientific activities across the
Overview In this role you will lead and evaluate managed access and named patient use requests from a clinical and ethical perspective, ensuring sound benefit–risk rationale. You will produce high-quality regulatory documentation and support global submissions across the
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 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, and
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 activities.
Overview In this role you will lead CDx regulatory strategy for pharmaceutical, biotech, and diagnostic programs. You will partner with cross-functional teams to align diagnostic development, biomarker strategy, and clinical trial plans with regulatory expectations and commercialization
Overview As Technical Specialist & Scheme Manager, you will support the certification of active medical devices for the European market. You will review technical and clinical documentation, manage certification activities, and provide regulatory guidance across CE marking schemes.
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 role you lead projects through the design and development process, acting as an expert in one or more competency areas. You mentor professionals, manage multiple initiatives from new product development to iterative improvements,
Overview In this role you help life science customers design, implement, and support LIMS within regulated environments, collaborating with cross-functional teams to deliver compliant laboratory solutions. You’ll shape project delivery from analysis to go-live and contribute
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 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
Work Flexibility: Hybrid or OnsiteWho we want:This position serves as a Manager of Professionals with project lead function, who advance through assigned projects along the design/development process and any legacy product care process. The advanced expert