Clinical Research Associate
Our Munich based client, specialising in manufacturing life-saving medical devices is currently looking for a CRA to support clinical project management through the duration of the study.
Some of the responsibilities will include:
Providing support in developing and writing clinical study documentation, while ensuring its compliant with the clinical study protocol as well as ISO 14155
Participating in co-monitoring visits as and when required at clinical sites in France, Germany & Belgium (once every other month)
Submission of study specific documents to regulatory authorities
Collating, filing and general administration of study documentation
Successfully completed technical or scientific studies or comparable qualification
Experience in working with medical device is essential
Working knowledge of the legal requirements for either medical devices or pharma, such as: ICH-GCP, ISO 14155
Excellent oral and written communication skills
Fluency in both German and English languages
Please apply with your CV or contact Kasia Krasuska for further details on this opportunity and additional vacancies in Regulatory Affairs and Quality Management.
+49 30 16 63 83 76