Clinical Trial SME

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries.

The role can be based in Dublin or Limerick.

Overview of the role

• 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.

Role Requirements

• 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.