Clinical Research Associate/ Senior Clinical Research Associate (SCRA)/(CRA)
An excellent opportunity has arisen for a Clinical Research Associate Senior Clinical Research Associate (SCRA)// Experienced CRAII (Clinical Research Associate) to work for an internationally recognised Clinical Research Organisation (CRO). This will offer you an excellent opportunity to learn and progress.
You will have the opportunity of participating in site selection process; perform evaluation of site capability and make recommendation for inclusion in clinical trial.
You will also be responsible for co-monitoring with junior CRA staff.
You will be an ambassador for the company and facilitate communication between allocated sites and key client line functions to increase value proposition to investigators.
For this role you MUST have prior monitoring experience in the UK, you must also have experience of monitoring a variety of phases and therapeutic areas.
If you would like to apply for this role you will ideally have the following:
Experience in clinical research and monitoring to ICH GCP is desired. (3 year plus)
A degree in a scientific or health care discipline preferred;
Personal qualities, skills and attributes must include the following:
* Knowledge and experience in international standards (including ICH GCP), and applicable international and local regulations.
* Expertise in communication, managing multiple priorities and computer literacy.
* Reliable and professional conduct.
* Excellent communication and influencing skills
For further information, call Bernardo Reveco on 0207 940 2105, or alternatively send you CV to email@example.com
CRA/ SCRA/ LCRA/ CRAI / CRAII/ clinical research associate / senior clinical research associate/ clinical monitor /clinical trials monitor / CRO/ clinical research organisation/ senior clinical research associate/ clinical monitor /clinical trials monitor / CRO/ clinical research organisation/ monitoring/ Clinical trials.
Posted: 29/07/2012 | NPJ Ref: 84514