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Job Description
As a Clinical Research Associate and under the supervision of the CRA Manager, you will ensure compliance of the studies conducted with ICH/GCP and country regulations, company policies and procedures, quality standards as well as adverse event reporting requirements internally and externally. You will act as the primary point of contact for the study sites and the site managers throughout all phases of the clinical research studies, taking overall responsibility of the allocated sites. On this rile you will actively develop and expand the territory for clinical research, finding and developing new sites and you will act as the subject matter expert for monitoring processes and systems.
Responsibilities
Qualifications
We offer an attractive salary, outstanding social benefits and an exciting work environment with varied tasks in an international environment. The minimum annual salary for this position is EUR 48.600,- and varies according to the qualifications and experience of the successful candidate. We are looking forward to receiving your application.
Current Contingent Workers apply
*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.
A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
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