Senior CRA/PM
Reference:
Job Type: Permanent
Location: United Kingdom, United Kingdom_Home based,
Salary: Competitive
Start Date: March 2012
Key Tasks:
- Carry out feasibility and advise Project Management regarding centre selection
- Attend and participate in Investigator Meetings
- Put together submits and tracks regulatory documents
- Set up and initiate investigational sites, ensuring all site staff are fully trained in trial protocol and conduct
- Monitor sites to ensure protocol compliance and patient safety to ICH GCP
- Perform SDV
- Query resolution
- Establish drug compliance
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