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Clinical Trials Associate

Integrated Resources, Inc North Wales Full-Time
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Essential Duties & Responsibilities:
1. Assist in preparations of recruitment projection and country site selection
2. Participate in study team meetings and collaborate with other Client functions, including preparation of meeting agendas and minutes
3. Participate in and assist in preparing meetings with the CRO and other vendors
4.
5. Assist in review of the study-related manuals and plans to ensure they are completed and revised as needed
6. Track expenses (direct and indirect) and support budget exercises
7. Assist in ensuring accurate and timely payment of invoices to the CRO and vendors
8. Assist in planning and preparing investigators, kick-off meetings and other GCO scientific meetings as needed
9. Review and maintain TMF required documents
10. File essential documents in SharePoint
11. Coordinating upkeep of Study Issue management tracker
12. Assist in activities related to study closure
13. Assist in coordinating CRO preparation and reviewing CSR appendices required for regulatory submissions
14. Prepare for ongoing audits/inspections and submission readiness
15. Any other task assigned by direct manager or the assigned project CPM and CRIM member

Position Requirements:
Education Required: College degree or equivalent work experience
Experience Required: At least 2 years of experience pharmaceutical industry or clinical research site based experience
Computer literate (Microsoft Outlook)
Fluent in English
 

Recommended skills

Research
Presentations
Pharmaceuticals
Timelines
Decision Making
Technical Services
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Job ID: 19-15668

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