My client is a global CRO who has a strong commitment to developing and training staff and allowing them to progress internally through the company. The company is experiencing such growth that they have a number of vacancies within the clinical research department and at present I am looking for a Clinical Research Associate (CRA) to monitor sites across the Nordics.
For this position, 2 years worth of experience in Clinical Research is essential and you will have done considerable site monitoring as a Clinical Research Associate (CRA). Special consideration will be given to those candidates who have done full lifecycle monitoring; including study start up and close out activities.
In this role, you will be responsible for running several clinical trials from study start to close. You will have sole responsibility for all aspects of the trials under your supervision. It is a great opportunity to master all aspects of a clinical trial and can be seen as an ideal stepping-stone to a career as project manager.
Brief description of tasks:
- Organise/supervise Clinical Trials
- Site selection/feasibility
- Monitoring visits
- Liaison with internal/external stakeholders
- Project management related tasks
The successful candidate will be entirely home based in this role, offering great flexibility in this role to control your own working hours and conditions. If this sounds like an ideal next step for your career then do not delay in applying!
I am currently working on behalf of a number of global and local organisations. Therefore, I offer confidentiality of approach from clients and candidates alike. To learn more about available opportunities, send your CV to H.Smithurst@nonstop-recruitment.com or call Holly Smithurst on +44 (0) 207 940 2105 for more information.