Senior Clinical Research Associate

Senior Clinical Research Associate Job Description Template

Our company is looking for a Senior Clinical Research Associate to join our team.


  • Maintain study specific files and documentation including device accountability (where applicable) and site files;
  • Assist with documentation preparation to support a clinical study;
  • Perform site qualification, site initiation, monitoring and study closeout activities of study centres (based across the UK);
  • Monitoring visits from feasibility through to close out;
  • Ensure that IRB/EC submission deadlines are met in a timely and accurate manner and documentation is filed;
  • Assist with the management of research studies including study site management;
  • Involved in preparation of submissions (regulatory, EC, protocol docs).


  • Life Science Degree;
  • At least 3 years of independent monitoring experience.