Clinical Research Associate (m/f)

Key Responsibilities

Evaluation, Initiation, Monitoring, Close-Out of national and International Studies
Supervision of the correct execution of medical research projects according to ICH-GCP as well as test- and monitoringplan
Guarantee the compliance of project targets
Close collaboration and communication with the study centers as well as continuous personal support of the investigators

Required Skills

At least 1 year experience as a CRA in initiation and monitoring of clinical studies at a pharmaceutical company or a CRO
Good understanding of ICH/GCP and regulatory requirements
Ability to effectively and unaffiliated performance of monitoring and all appropriate activities
Willing to travel
Poise, authority and clear communication
Good knowledge of MS-Office Products
Very good knowledge of English and German Language
Further foreign languages would be beneficial

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send your documents to:

Inamed GmbH
Human Resources
Robert-Koch-Allee 29
82131 Gauting
Germany