Clinical Research Manager coordinating clinical studies from planning to publication for digital health solutions. Ensuring compliance, conducting analyses, and collaborating interdisciplinarily.
Responsibilities
You support clinical studies from planning to publication, including documentation, reporting, and stakeholder communication.
You create and maintain regulatory documents (in particular Clinical Evaluation and PMCF) and professionally prepare the study data required for these.
You independently produce scientific background materials through structured literature searches and data analyses, and you write reports and manuscripts.
You process complex datasets and contextualize them for scientific and regulatory questions, in close coordination with Regulatory Affairs and Data Science.
You provide scientific support for funded projects and research collaborations, from identifying suitable formats to the dissemination of project results.
Requirements
Degree in medicine, health sciences, or natural sciences (Master’s/PhD advantageous)
Some to several years of experience in clinical project management or in research projects
Understanding of regulatory requirements for digital health applications (e.g., GCP, MDR, ISO 14155, DiGAV)
Structured, reliable, and analytical working style
Enthusiasm for interdisciplinary collaboration and scientific quality
Excellent German and English skills, both written and spoken.
Benefits
Diverse professional and personal development opportunities, with space for your own ideas
The option to work remotely for up to one month per year from the EU, EEA, or Switzerland
Access to corporate benefits with attractive employee discounts
Company pension plan for financial security
30 days of vacation for your recovery
An open, dynamic, and appreciative corporate culture
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