Clinical Research Associate

Sourcia is a full service CRO deploying a unique model to serve our clients; small to medium-sized Bio- and Med tech. We have offices in Munich (Germany), Zevenbergen (the Netherlands) and Ghent (Belgium) and operations throughout Europe.

We are growing and are looking for new colleagues at our offices in Munich as well as Zevenbergen:

Clinical Research Associate

As Clinical Research Associate (f/m/n) you are a crucial part of our project teams and will be responsible for site management and monitoring in our international clinical trials. 

 

 

Work activities include:

 

Your profile:

       Contact with the Ethics Committees / Regulatory Authorities

       Identifying and assessing the suitability of clinical sites and identifying investigators (feasibility)

       Setting up the trial sites, training the site staff to trial-specific industry standards;

       Monitoring the trial throughout its duration

       Supporting clinical trial documentation and Trial Master File management

       Degree in Life Science or equal experience in clinical development / monitoring

       Understands and can apply knowledge of clinical trial designs to trial execution

       Advanced knowledge and experience with GCP/ICH and local regulations

       Strong communication skills

       Excellent organizational skills with high attention to detail is required

       Ability to manage, prioritize, and routinely report progress on multiple projects and tasks

       Strong presentation skills to internal professionals and external collaborators

 

 

We are looking forward hearing from you – please send your application to info@sourcia.eu

 

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