Homebased - Permanent
Salary: up to £50,000 (D.O.E) plus benefits
A leading CRO, focused on the development of innovative new therapies to improve the world’s health, is looking for a Senior Clinical Research Associate to work within their Real World Evidence team.
Key Responsibilities
- Site management and monitoring including selection, initiation and close out visits
- Adapt, drive and track subject recruitment plan across sites
- Collaborate and liaise with study team members and key study personnel.
- Manage study progress through completion and quality of relevant documentation, including supporting the start-up phase.
- Create and maintain monitoring visit reports and action plans
- Ensure full ICH-GCP and regulatory guidelines followed throughout study.
- Supporting subject recruitment plan and site financial management as required.
Key Requirements
- Life science degree
- Minimum of 12 months independent on-site monitoring experience within the UK
- Good therapeutic and protocol knowledge across a range of areas.
- Strong ICH-GCP and UK regulatory knowledge
- Full UK Driving license
If this role is of interest, please send your CV to [email protected] or call 0118 952 2793.