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Job Description
As a SrCRA you will be part of a very engaged team ensuring excellent studies and high site performance. Clinical Research at Our Company is given top priority and is a cornerstone of the business. Consequently, you will as a SrCRA have considerable responsibility.
As SrCRA you play an important part in ensuring performance and compliance with ICH/GCP and country regulations for assigned studies and sites. In your role you will act as the primary site contact and site manager, taking the overall responsibility of allocated sites.
Finally, as one of our fast-paced and resourceful SrCRA you will also be actively developing and expanding the territory for clinical research – including finding and developing new sites.
Furthermore, we are looking for a colleague that:
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.
07/01/2024
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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