Senior Clinical Research Associate - Clinical Operations
- Experience Level
- Experienced (non-manager)
Covance is looking to recruit a home based SCRA to work within tour clinical operations group. This role exists within the general medicine/biopharma part of the internal clinical operations department and does NOT include Oncology which is a different entity within the company.
You would be responsible for Site management and monitoring responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP from site selection to close out
You would be responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned.
This is a National monitoring role but monitoring schedules are realistic and allow for a work life balance
Overnight stays may be needed on occasion.
There are excellent opportunities for career development within this group.
Please contact Marc Joseph on 01753 216664 or send your CV to email@example.com
key words clinical research associate, CRA, monitoring, site management, clinical trials