Clinical Project Lead
Posted on Mar 17, 2019 by Hobson Prior
Develop and/or review specific study-related documents
Coordinate preparation of study-related documents
Support process of Trial Site Selection
Support / Coordinate submission to Competent Authorities (CA) and Ethical Committee (EC)
Trial Set-up Activities
Project Management & Administration
Other Clinical activities as directed by the VP Head of Regulatory and Clinical Affairs
5 + years' experience in managing clinical trials in Medical Device industry (Class II B implants) plus experience in pharmaceutical clinical affairs
Master's degree in Life Sciences
Attention to details
Flexibility (travel from 25% up to 50% of time)
Knowledge in ophthalmology is a plus
Fluency in English
Good knowledge of GCP
Good communication, prioritization, organizational and time management skills
Team player with positive constructive attitude to solve problems
Eager to learn, stress resistant, Strong self-development abilities and able to work independently.
If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.
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