What are the responsibilities and job description for the Clinical Study Coordinator position at Redbock - an NES Fircroft company?
A leading medical device company is seeking a Clinical Study Coordinator to support their group with management of clinical study documentation and data. This position will be performed on site in Minneapolis, MN.
Candidates can and should be mostly entry level, although candidates with previous exposure to clinical research, academic research, or clinical care experience will be strongly preferred.
This candidate will function as an entry level administrative resource supporting clinical operations and coordinating collection and documentation of clinical data.
Clinical Studies Support Coordinator II (24-month contract // Minneapolis, MN):
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 - $25
