Clinical Studies Support Coordinator

Clinical Studies Support Coordinator II (24 month contract // Minneapolis, MN):

HM's Top 3:

1. Proficiency in MS Office applications (Excel, PPT, Word, web-based applications)
2. Clinical research, academic research, or clinical care experience preferred.
3. Experience with GCP, regulatory and/or compliance guidelines for clinical trials (nice to have).

Education Required: Bachelor’s degree with 0 years of clinical research experience.

Years’ Experience Required: 0 years of Clinical Research Experience Required

Duties:

• Supports clinical studies by executing and maintaining one or more of the following areas:
• Data coordination: actively participates in the development and testing of case report forms, study reports, and study databases based on protocol requirements.
• Ensures timely and quality completion of data forms; verifies study data; and generates, manages, and resolves data discrepancies.
• May process compensation & identify and resolve compensation discrepancies.
• Document coordination - creates and manages the clinical study files and oversees the organization and distribution of clinical study documents.
• Assists with periodic audits of clinical study files for completeness and accuracy.