Clinical Studies Specialist
North Chicago, IL
- Managing the Trial Master File (TMF), ensuring documents maintained in the file are appropriate and the content of those documents is accurate, complete and consistent with AbbVie SOPs and regulatory requirements.
- Support clinical team, primarily in tracking, organizing and filing Phase I-IV study documents according to Federal Regulations and ICH guidelines.
- Assist Clinical Team members in handling data queries, drug inventories, study invoice payments, enrollment tracking, and record reconciliation with site documents.
- Assists the CRAs with organizing and planning study investigator meetings.
- 3-5 Years Experience Level.
- Bachelor s degree is required.
For more information, please contact A-line Staffing Solutions at 877-782-3334.