| Job Title: CRA Registry Coordinator |
| Description |
| Our client is a Pharmaceutical company that currently have an opportunity for a CRA Registry Coordinator
Responsibilities will be to coordinate a disease registry throughout Europe. Duties - Site set-up, ethics submission, site management and monitoring as well as maintenance and training on EDC system
- Coordinates or supports the clinical trial submissions to the Competent Authorities, Main Ethics Committee, Local Ethics Committees and other relevant boards
- Coordination of registry meetings
- Conducts site initiation visits, periodic monitoring, and site management
- Good Clinical Practices/International Conference on Harmonization etc
- Assists in activities related to audits and regulatory inspections.
Requirements- Clinical monitoring experience or registry experience
- Detailed knowledge of drug development, ICH/GCP Guidelines and knowledge of regulatory requirements
- Experience with EDC
- Strong interpersonal skills and teamwork
- Ability and willingness to travel internationally
- Bachelor's degree, nursing diploma or equivalent.
Please note that only candidates with EU work authorisation will be considered. |
| Details |
| Post Date: |
03/11/2009 |
| Hours: |
Full Time |
| Location: |
United Kingdom |
| Working Term: |
Permanent Position |
| Salary: |
£30,000 to £35,000 |
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