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.