CERES GmbH evaluation & research is a successful and growing company in southwest Germany. We organize and conduct clinical investigations for medical device manufacturers, provide medical writing services, and performe clinical evaluations for medical devices.
Our employees obtain responsibility appropriate to their position. Self-reliance, preciseness as well as friendly and respectful treatment amongst colleagues and with executives characterize our company culture. We encourage our employees to contribute to a steady improvement of our company.
To work at CERES, academic or work experience relevant to clinical research with medical devices, the ability to work well both independently and with a team, excellent communication skills, and fluency in both English and German are essential. Fluency in other European languages is desirable.
If you would like to work with us, please send your complete application (cover letter, CV, relevant documents) to info [AT] clinical-evaluation.com .
Clinical Trial Manager
- Planning, initiation and management of clinical investigations in various indication areas
- Coordination and training of internal and external project members
- Cooperation with clients, external experts as well as advice and development of customer and product-specific solutions
- Participation in the compilation of study-related documents: investigator brochure, applications for authorities and ethics committees, etc.
- Ensuring regulatory requirements
- Resource planning
- Contribute to (S)AE management
- Participation in strategic, professional and personal development
The full job advertisement is available here: Clinical Trial Manager .
- Editing and review of medical device documentation
- Creation and editing of study-related documents and registration dossiers. These include: clinical investigation protocols, investigator manuals, final reports, applications at competent authorities and ethics committees, etc.
- Participation in and preparation of clinical evaluations for medical devices
- Research as part of the projects
- Project planning
The full job advertisement is available here: Medical Writer .
Clinical Research Associate
The full job advertisement is available here: CRA .
- Source data verification in the participating sites
- Site initiations and close outs
- Participation in the planning, preparation and initiation of clinical investigations in various indication areas
- Compilation of the study-relevant documents
- Applications to authorities and ethics committees
- Project-related support
- Planning and implementation of data management for clinical investigations according to MDR requirements.
- Identification and solution of operational problems / processes in order to reach study milestones promptly and appropriately.
- Ensuring data quality, consistency and integrity.
- Analysis of the consistency of study data and results.
- Data transfer and reporting.
- Conception, creation and validation of study databases.
- Realization of case report forms (CRFs) according to the test plan and SAP.
- Coordination of data management.
- Participation in clinical studies in cooperation with project management, monitoring and biometrics.
- Cooperation with clients, external experts and the development of customer and product-specific solutions.
The full job advertisement is available here: Data Analyst .