What are the responsibilities and job description for the Clinical Studies Support Coordinator II position at Redbock - an NES Fircroft company?
Clinical Studies Support Coordinator II (24-month contract // Minneapolis, MN):
Join a leading medical device manufacturing company as a Clinical Studies Support Coordinator. The team is seeking individuals to support their group with management of clinical study documentation and data, ideally having previous exposure to clinical or academic research.
Candidate's will either be on-site in Mounds View or Rice Creek. W2 Candidates only****
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.
Salary : $20 - $27
