Clinical Trial Assistant - Thüringen, Deutschland - Vertraulich

Vertraulich

Geprüftes Unternehmen

Thüringen, Deutschland

vor 3 Wochen

Geschrieben von:

Lena Wagner

beBee Recruiter

Beschreibung

Support in conduct of clinical studies and registries according to all applicable regulations, to commonly accepted practices, and to the company internal guidelines

Preparation and maintenance of the sponsor file

Preparation of study-specific documents

Support of Clinical Project Management with any study activities

Track record of study documents

Preparation of meetings and creating protocols

Assistance with study audits, if required

Contribution to the overall tasks of the Clinical Research Department

Performance of other related duties and responsibilities as assigned

Anforderungen

Knowledge of regulatory clinical research framework, standards and guidelines

Excellent English skills, verbally and in writing

Fluent German, verbally and in writing

Professional experience in medical device industry and/or clinical research

Strong analytical and problem solving skills as well as Hands-on working

Proven track record of working in a dynamic, international environment

Excellent skills in relevant software programs ( MS office, CTMS)

Wir bieten

The company will offer you an interesting job in a team of people who like to work together and always focus on helping our customers to save and improve patient's lives with innovative and highest quality products.

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