- You will understand the scientific basis of assigned clinical trials and be able to communicate this effectively to other team members, investigators, and site staff.
- Your responsibilities will also include identifying effective prescreening strategies for each trial and recommending improvements.
- A minimum of 12 months' experience in the clinical research environment as an employee of a research site, sponsor, or biotech/pharmaceutical company is required.
- You must have read write speak fluent English fluency language ability skills
- A Doctorate degree PhD PharmD MD DO DPN from biological science field related area required travel willing up % }
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Associate Clinical Trial Liaison - Perugia - ICON plc
Descrizione
Associate Clinical Trial Liaison
We are seeking a highly motivated Associate Clinical Trial Liaison to join our team at ICON plc. As a key member of our study team, you will develop relationships with clinical trial investigators and research site staff to facilitate recruitment of subjects in pharmaceutical industry clinical trials.
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Process Specialist
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