We are currently searching for a skilled professional to join a well-known client’s team as a Clinical Studies Support Coordinator II in Rice Creek or Mounds View, MN. The Clinical Studies Support Coordinator II role provides organizational and administrative support to ensure the successful execution and maintenance of clinical studies. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity.

RESPONSIBILITIES
Data Coordination:
• Actively participate in the development and testing of case report forms, study reports, and study databases based on protocol requirements.
• Ensure timely and accurate completion of data forms, verify study data, and manage data discrepancies.
• Generate, review, and resolve data queries to maintain data integrity.
• Process participant compensation and identify/resolve any related discrepancies.
Document Coordination:
• Create, manage, and organize clinical study files.
• Oversee the distribution and tracking of clinical study documents.
• Conduct periodic audits of clinical study files to ensure completeness and accuracy.
Office Support:
• Provide clerical and administrative support for the clinical study team.
• Communicate with internal stakeholders to obtain and provide information requiring some explanation or interpretation.
• Identify and propose solutions to routine problems in work processes or systems.

EDUCATION
Minimum of Bachelor’s Degree in a related discipline required

To be a best-fit your strengths must include:
• 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)