Clinical Trial SME
Talent Acquisition Business Partner
- Full Service Division
About the role
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- Review clinical trial protocols and identify possible vulnerabilities and present your findings to the production team using you clinical knowledge and experience to provide direction for the project.
- Attend meetings with the clients as needed and attend daily team scrums and provide clinical input as needed on all study components.
- Provide the clinical guidance and expertise necessary to assist in the production of our product offering in particular drawing on experience from on-site monitoring and daily interaction with clinical sites.
- Technically review all production scripts to ensure technical accuracy and relevance to the end user (i.e. Investigators and Site Staff).
- Work closely with the project PM to ensure the delivery of an on-time and high quality product beneficial to those who work on the trial and ensuring maximum usage by the end user.
- Ensure the maintenance of a high personal level of knowledge concerning current regulation and changes within the clinical research industry by means of internal support and individual learning.
- B.Sc. (Hons) in life science or equivalent.
- At least 2 years’ experience as a Clinical Research Associate/site monitor or equivalent within the clinical research industry.
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
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