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Section: Science Vacancy 741 |
| Post:Clinical Trials Assistant
|
Salary contractual |
| |
| Requirements and conditions |
| Age: |
Has no value
|
| Gender |
Has no value
|
| Education: |
no
|
| Work schedule: |
Has no value
|
| Work place: |
Southampton
|
| The announcement text: |
A well respected CRO has an urgent requirement for a CTA to be based in their offices in the M4 Corridor
Key duties include:
• Provide clinical support for projects according to company Standard Operating Procedures, ICH Guidelines and GCP.
• Develop and*or maintain tracking systems for clinical projects.
• Assist in field monitoring responsibilities
• Act as contact for project team and study sites.
• Perform CRF review, query generation and resolution against established data review guidelines
• Assist with generation and reconciliation of queries to investigative sites*clients to resolve problem data.
• Assist with the management of study supplies and organize shipments.
• Update, track and maintain study-specific trial management tools*systems.
• Co-ordinate meetings with clients, investigators and project team, including taking minutes
• Assist in submissions and notifications to Ethics Committees and Regulatory Authorities.
|
| Contact information |
| Employer: |
|
| Email: |
|
| Phone: |
01252 615100
|
|
| |
Publication date: 2009-03-29 12:37:44
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