As CRA you will be responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits. Other duties will include negotiating study budgets with potential investigators, assist with training, mentoring, and development of junior employees, e.g. co-monitoring (for CRAs II and SCRAs).
In return, we offer you the opportunity to develop your career with an international organization; to pursue further training and to take advantage of our flexible conditions and attractive remuneration package.
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