ICON Clinical Research

Clinical Trial SME

Location
Dublin
Salary
Competitive
Posted
22 Feb 2021
Closes
03 Mar 2021
Ref
JR070555
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
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.