Clinical Research Spec - Exempt

Join our team as a Clinical Research Specialist and play a vital role in advancing medical research and innovation. We are seeking an experienced professional to oversee, design, and develop clinical evaluation research studies. This full-time, onsite position is based in the vibrant community of Mounds View, MN, offering a blend of suburban charm and proximity to urban amenities. Key Responsibilities Oversee, design, plan, and develop clinical evaluation research studies. Prepare and author protocols and patient record forms. Conduct registered and nonregistered clinical studies of products with medical need or commercial potential. Interpret results of clinical investigations for new drug devices or consumer applications. Resolve operational aspects of clinical trials in conjunction with project teams. Ensure compliance with SOP, GCP, and specific country regulations. May prepare clinical trial budgets and manage clinical supply operations, site, and vendor selection. Qualifications Bachelor's degree required. Minimum of 2 years of experience in clinical research. Site management experience (site or sponsor) is essential. Knowledge/experience with CTMS/EDC/TMF systems. Proficient understanding of Good Clinical Practice (GCP). Skills and Attributes Ability to work independently with general supervision on larger, moderately complex projects. Strong communication skills to interact primarily with internal contacts. Problem-solving skills to address general issues and improve job area effectiveness. Capability to provide guidance and mentorship to entry-level professionals. Embrace this opportunity to contribute to meaningful projects and be part of a supportive and innovative team. Apply today and make a difference in the field of clinical research.

Created: 2026-04-15