Description
A leading global health care company are looking for a Senior Clinical Research Associate (SCRA) on an intial 9 month contract with the view to being extended. This is an office based role in Oxfordshire but there is potential for some home working.They will be running CE trials so will be looking for someone who has experience of running clinical trials within Medical Devices.
Some of the key responsibilities include:
-Site monitoring responsibilities for clinical studies according to SOPs, -ICH Guidelines and GCP.
-Attend and Participate in investigator meetings.
-Manage study budgets and contracts including negotiations.
-Look after more junior CRAs.
-Identify new investigators for future studies.
-Review CRF's and provide relevant feedback
-Assist with IRB/IEC submissions as required.
-Attend study team meetings
Monitoring experience.
Experience in the use of project management tools .
Demonstrated understanding of the field of Diabetes.
Previous working experience of the European or US regulations/standards affecting clinical studies for Medical Devices or IVDs.
If you are interested in this role please respond ASAP with an updated CV and your location and availability to start and to interview.
Please pass this on to friends or colleagues as we offer referral vouchers.
Thanks and regards,