Werde Clinical Trial Project Assistant (m/w/d) bei Dr Regenold GmbH in Badenweiler – Dein Traumjob wartet auf dich

Do you want to work with us?
Then we should get to know each other!

we are looking for an individual as soon as possible who can ...

Clinical Trial Project Assistant (m/f/d)
Full-time / Part-time

who we are and what we do
Founded in 1994, regenold GmbH is an international regulatory service provider with over 100 employees. We
support clients worldwide in the development, approval and market access of pharmaceuticals, medical devices
and in vitro diagnostics, cosmetics, food supplements and other healthcare products.
You can find more information on our homepage: www.regenold.com

your responsibility
your tasks will include 

cooperation with the project team with accurately updating and maintaining clinical tracking systems 
responsibility for the preparation, handling, distribution, collection, filing, and archiving of clinical

documentation and reports according to the scope of work and the SOPs 
keeping yourself professionally abreast of all regulatory and operative aspects relevant to the clinical

projects you will be assigned 
knowledgeable, following appropriate training, in the application process for clinical studies, in force in the

country(ies) of work. Accordingly, you can be required to provide updates on the applicable regulation for
the application process in the country of work, whenever relevant 

preparation and request of the necessary local authorities' approvals 
support of the project team in managing the agreements with hospitals and investigational centers 
collaboration with the project team on the preparation, handling and distribution of clinical trial supplies and

maintenance of tracking information (logistics of the project) 
collaboration with the project team in organizing investigator and Monitor Meetings 
collaboration in complying with and enforcing company procedures

your education, skills, knowledge and experience 

High School Diploma 
Ideally two (2) years of clinical research experience in the CRO/Pharmaceutical industry 
Good Knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory

requirements 
Excellent written and oral communication skills in German and English 
Proficiency in Microsoft Office (e.g., Word, Excel, Outlook) 
Good organizational abilities, ability to prioritize and multitask

our value promise 

Customer and solution orientation - for us, this is the DNA of a good service provider 
Experience, expertise and worldwide networking in over 90 countries through the regulanet® network,

www.regulanet.com 
Innovative and long-standing customers who are happy to recommend us to others 
a cross-team personal and active, lively teamwork 
an attractive, bright and modern working environment

what you get 

International diversity - in the team and in the projects 
Long-term prospects - for professional and personal development, we offer a wide range of tasks and

individually tailored training opportunities right from the onboarding phase 
Flexibility, freedom and personal responsibility - through flat hierarchies, short decision-making processes

and family-friendly working time models, with something for everyone … 
One of the most beautiful regions in Germany, also called the Toscana of Germany, on the edge of the

Black Forest in the border triangle of Germany/ France/ Switzerland 
Attractive salary, company pension scheme, capital-forming benefits, JobRad, Hansefit, Shuttle Transfer

Freiburg-Badenweiler and much more, promised…

Did we make it? Curious?
Then we look forward to receiving your complete application to
perspectives@regenold.com
Contact Christine von der Brelie / +49 (7632) 8226-410
regenold GmbH / Zöllinplatz 4 / 79410 Badenweiler / www.regenold.com