Biology, Case Report Form (CRF), Clinical Research, Clinical Support, Clinical Trial, Cross-Functional, Data Collection, Diabetes, Documentation, Electronic Data Capture (EDC), GCP (Good Clinical Practices), Maintain Compliance, Operations Management, Problem Solving Skills, Regulations, Regulatory Compliance, Standard Operating Procedures (SOP)
Job Title: Clinical Research Specialist (Job ID: 25225)
Location: Mounds View, MN (Onsite)
Duration: 24 Months
Pay: $35–$40/hr
Role Summary
Clinical Research Specialist supporting clinical trial operations, site management, and study execution in compliance with GCP and regulatory standards.
Must-Have Skills
- Site management experience (site or sponsor side)
- Experience with CTMS / EDC / TMF systems
- Strong knowledge of Good Clinical Practice (GCP)
- Clinical trial operations experience
Nice to Have
- Diabetes therapeutic area experience
Key Responsibilities
- Support clinical study planning, design, and execution
- Prepare protocols, CRFs, and study documentation
- Manage site operations, vendors, and clinical trial activities
- Ensure compliance with GCP, SOPs, and regulations
- Monitor and resolve trial operational issues
- Support data collection, reporting, and study closeout activities
- Coordinate cross-functional clinical project activities
Experience Required
- Bachelor’s degree (Life Sciences/Medical preferred)
- 2+ years clinical research experience (or 0 with advanced degree)
- Experience in clinical trials / site operations required
Work Setup
- Onsite (Mounds View, MN)
- 40 hours/week