天津招聘

Job Description：

Monitor multiple Phase II/III clinical trial sites, across therapeutic areas. Assist other CRA with co-monitoring activities both remote and on-site as needed.
Target 5-10 site assignments (depending on complexity/enrollment/stage of study), average 2-3 protocols and 1-2 therapeutic areas at any given time. The number would be adjusted based on the workload assignment.


Requirements:
-Must have a Bachelor's Degree (or equivalent)
-Minimum 1 years of monitoring and site management experience.
-English is workable, along with proficiency in the use of Microsoft Office suite.

We are a global provider of consulting, and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas. ICON has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.