Clinical Studies Support Coordinator II (24 month contract // Minneapolis, MN):
HM's Top 3:
Proficiency in MS Office applications (Excel, PPT, Word, web-based applications)
Clinical research, academic research, or clinical care experience preferred.
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.