We are hiring
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.
Vacancies (m/f/d)
We currently have no vacancies.
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 
.
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
Your Responsibility
- Developing of regulatory & clinical research strategies for planned clinical trials
- Working with competent authorities, ethics committees, international study teams & sponsors
- Understanding customer needs & building collaborative customer relationships
- Preparing & handling of essential study documents
- Reviewing design history files, literature & compiling investigator brochures
- As an expert, contributing with innovative ideas to continuously improve and expand our services
The full job advertisement is available here: Clinical Trial Manager .
Scientist, Physician or Medical Engineer (m/f/d)
as Clinical Research & Regulatory Affairs Manager – CRO
Your Responsibility
- Developing of regulatory & clinical research strategies for planned clinical trials
- Working with competent authorities, ethics committees, international study teams & sponsors
- Understanding customer needs & building collaborative customer relationships
- Preparing & handling of essential study documents
- Reviewing design history files, literature & compiling investigator brochures
- As an expert, contributing with innovative ideas to continuously improve and expand our services
The full job advertisement is available here: Clinical Research & Regulatory Affairs Manager
Medical Writer
Your tasks
- Editing of clinical evaluations for medical devices
- Processing of study-relevant documents and applications for approval with authorities and ethics committees
- Implementation of regulatory requirements for medical devices in the area of approval and market surveillance
- Coordination of internal and external project participants
- Cooperation with clients, external experts as well as consultation and development of customer- and product-specific solutions
- Participation in the professional and strategic development of the company
The full job advertisement is available here (DE): Medical Writer
Clinical Research Associate
The full job advertisement is available here: CRA .
Your tasks
- 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
Clinical Research Associate
Your tasks
- 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
The full job advertisement is available here: CRA.
