天津招聘

The role
? Responsible for performing feasibility, site identification, site contract negotiation, and other SSU activities.
? Provide country specific SSU expertise to Study Start Up team leads and project teams.
? Responsible for the preparation and coordination of submissions to regulatory, ethics, and other bodies.
? Develop, finalize, and review Master and Country Specific Subject Information Sheets/Informed Consent Forms.
What you need
? A Bachelor’s Degree or local equivalent and/or appropriate experience from the Medical/science background and/or discipline.
? A minimum of 1 years of experience or understanding of clinical study start up requirements and activities.
? Fluency in the local language and English is essential.

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.