Klinikai kutató állások, munkák

The Research and Development Department is responsible for the continuous expansion and optimization of our in vitro assay portfolio, including but not limited to drug transporter-related assays and complex in vitro models and new approach methodologies. Running contract research projects to...

• Respective specialities: ecotoxicology, in vitro toxicology, genetic toxicology
• Key role in management of preclinical studies or regulatory toxicity studies
• Study set- up, study plan, study conduct and supervision

• Support GxP compliance of all activities in the clinical trial supply management, drug-related distribution and storage
• Responsibility for the project-related GxP documentation and maintenance of lists

• Interpret and apply global technical and scientific regulations related to products, ingredients, and materials across different markets
• Collaborate closely with SRA, R&D, and Legal teams (HQ and local markets) to monitor and assess regulatory developments

Global Project Manager Global Project Manager: Project Manager / Drug / Combination Products Medical Device / Pharmaceutical / Biopharmaceutical / Smartsheet / 21CFR820.30 / Design Control requirements / PMP / English / German Background: We are looking for a Principal Project Manager (PM) to...

Supervise collaborations: Conduct feasibility projects with customers, universities and internal collaborators....

• Management of all clinical operational and quality aspects of allocated studies of moderate to high complexity in compliance with ICH GCP
• Assumption of Lead CTM responsibilities on regional level or Clinical Study Manager responsibilities

• Facilitation of site start up and communication with internal and external team members
• Support of sites and study teams to achieve rapid site start up
• Work directly with assigned sites on all site related essential document collection and review

Design and implement end‑to‑end Operations and Supply Chain strategies across the Life Sciences value chain – from R&D to manufacturing, supply, and quality....

Establish requirements, ensure that the underlying clinical rationale and supporting literature are documented, and identify any conflicting or shared requirements across teams and projects...

• Identify, analyze, and continuously improve processes across Science operations
• Drive the development of robust and future-oriented process solutions and standardize best practices
• Define and track KPIs and build dashboards and performance reviews together with operational teams

• Lead the initiation of new products and manage the full product lifecycle of existing solutions in audiometry, tympanometry, OAE, and ABR
• Analyze customer and market needs through interviews, on-site visits, and third-level support activities

Support of planning, managing and steering of timelines, costs and scope of Trial Teams for agreed deliverables of global supply chain activities for assigned clinical trials, including highly complex trials...

• Develop IRT System specifications to meet the needs of the study design in collaboration with Clinical Trial Supply Unit (CTSU) functions, Medical, Clinical Data Management and Biostatistics
• Select IRT Vendor and create study specific contract

Responsible for global Supply Chain activities for Investigational Medicinal Products (IMPs) of national and international Phase I-IV clinical trials in the Therapeutic Area General Medicine...

Provide scientific leadership for AI-powered computational pathology and multimodal biomarker development across AstraZeneca's Oncology and/or BioPharmaceuticals portfolio, delivering biomarkers that support patient selection and translational decision-making from target validation through clinical...

Senior HEOR Manager Patient-Reported Outcome (12 months contract) m/f/d At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is nolonger a dream, but a real possibility. We're doing it with energy, curiosity and...

What you'll build You'll define the technical direction for secure, scalable interoperability between Hospital Information Systems (HIS) and the SAP portfolio, helping healthcare providers seamlessly connect clinical and business processes across the enterprise. Working closely with strategic...

• Conduct an independent, hypothesis-driven research project on the role of MiT transcription factors in neuroinflammation and autoimmunity
• Process and analyze primary human and mouse samples
• Perform EAE experiments, including disease monitoring and sample collection

• Analyze and interpret clinical study data using appropriate statistical methods
• Provide statistical expertise in the design and planning of clinical research studies, including sample size determination