Careers
Global Expertise, Personal Touch
Your career at Eurofins bioskin
Join the Eurofins bioskin team!
We believe that our employees are our most valuable resource!
Eurofins bioskin offers the opportunity to personally grow, to increase individual expertise and to broaden experience. We are committed to providing our team with the tools, resources, and encouragement to reach professional goals.
Eurofins bioskin offers a working environment that is based on trust, respect and common values.
As member of the Eurofins bioskin team you benefit from:
- Training plans for an excellent start
- Flexible working hours with models that range from flex-time and part-time to home office opportunities finding an optimal balance between the needs of the employees and the requirements of the company
- Continuing education and training
- Company pension plan plus company supplement
- HVV Profiticket with company supplement
Would you like to work in the middle of the Hamburg Altstadt in the direct neighbourhood of the world cultural heritage Chilehaus, and in within eyeshot of the Speicherstadt and Hafencity/Elbphilharmony in walking distance? Here, right next to the "Messberg" subway station or even just a 10-minute walk to the main train station "Hauptbahnhof" you can find lots of places for a perfect lunch break in many different restaurants. Our modern offices, designed for 2-4 people, are in the Danske Hus, which of course has a bicycle cellar in the underground garage for employees who want to come to work by bike.
It's a perfect working environment in a great team in the most beautiful area of the most beautiful city!
If there are no current vacancies or your position is not listed below, you are always welcome to send us an unsolicited application to:
Eurofins bioskin GmbH
Messberg 4, 20095 Hamburg, Germany
Phone: +49 40 6068970
SM_bioskin-recruitment@cpt.eurofinseu.com
Junior Clinical Research Associate (CRA)
We are looking for a Junior Clinical Research Associate (CRA) to join our team at bioskin in Hamburg. The CRA's essential function is to act as a link between sponsor, CRO and trial site as well as the quality control of early phase clinical trials in-house at bioskin as well as multicenter trials at the sites in Germany or other German-speaking countries.
Focus of tasks:
- Performing and reporting site monitoring visits, including site selection, initiation, periodic and close out visits for clinical trials phase I-IV in Germany
- Ensuring adherence to international standards (e.g. ICH-GCP), standard operating procedures and clinical trial protocol
- Maintaining investigator site files
- Assessing on-going training requirements of all sites staff and take appropriate action
- Identifying and escalating protocol deviations, discrepancies in data, and non-compliance to clinical trial protocols
- Working with different types of eCRF, CTMS systems
- Feasibility of sites
- Collection of essential documents, review, and maintenance
- Close cooperation with the different departments in-house at bioskin as well as vendors/freelance CRAs
- Preparation and mailing of investigator folders.
- Assist in compiling documents for filing in the paper-based TMF or uploading documents to the electronic TMF.
- Review documents collected by other CRAs for accuracy and completeness as required by the DIA Model or Trial Master File Plan.
- Preparation or compilation of documents relevant to the trial for monitoring purposes
Profile:
- Degree in a scientific or medical discipline or equivalent
- At least 1 year of experience as a Clinical Research Associate (including travelling) are imperative, ideally including multicenter and multinational trials
- Familiar with ICH-GCP guidelines, regulatory requirements, monitoring procedures and understanding of the clinical trial processes
- Experienced in medical device clinical trials and the applicable regulatory requirements would be an asset
- Well-structured and organized, target-oriented personality, team player
- Ability to thoroughly solve problems and issues
- Fluent in German and English (written and spoken)
- Ability and motivated to travel, including overnight stays
- Competent with MS Office applications
- Candidates with experiences in the indication dermatology will be preferred
- Located in Hamburg
Please send your application including your anticipated salary to:
Eurofins bioskin GmbH
Messberg 4, 20095 Hamburg
Bettina Möhlenbrock
SM_bioskin-recruitment@cpt.eurofinseu.com
Study Nurse (w/m/d)
Focus of tasks:
- GCP-compliant collaboration in clinical studies
- Assisting the investigators
- Carrying out study-specific tasks in the non-medical area (vital signs, blood sampling, application of test medication, use of instrumental measuring methods, etc.)
- Collection and documentation of clinical data in the subject file and CRF/eCRF
- Administration of study documents and trial medication
- Preparation and assistance with monitor and auditor visits
Your profile:
- Completed training in a medical assistance profession
- Additional qualification as a study nurse would be desirable
- If possible, experience in conducting clinical trials
- Preferably previous experience in the field of dermatology
- Good written and spoken English skills
- Very good communication and teamwork skills
- Sense for structured work and organizational talent
Please send your complete e-mail application as a PDF file with salary expectations to:
Eurofins bioskin GmbH
Messberg 4, 20095 Hamburg
Bettina Möhlenbrock
SM_bioskin-recruitment@cpt.eurofinseu.com
