Clinical Project Manager in Salt Lake City, Utah at SAON

At SAON, we are committed to advancing clinical research that improves patient outcomes and supports the future of musculoskeletal care. We are seeking a Clinical Project Manager to lead the operational execution of clinical studies from study start-up through closeout while ensuring the highest standards of quality, compliance, and data integrity.

In this role, you will partner closely with investigators, research sites, and internal stakeholders to drive study success. You will oversee study timelines, site activation, monitoring activities, data quality, and regulatory compliance while proactively identifying and resolving operational challenges. The ideal candidate is an organized, collaborative, and solutions-oriented clinical research professional who thrives in a fast-paced environment and is passionate about delivering high-quality research.

This remote position offers the opportunity to make a meaningful impact while working alongside a team dedicated to innovation, scientific rigor, and excellence in clinical research. Up to 10% travel may be required.

Benefits Offered:

• Paid Vacation Time Off
• Paid Sick Time Off
• 9 Paid Holidays + 2 Floating Holidays
• Health, Dental and Vision Insurance
• Company Paid Life Insurance
• Company Paid Short-Term and Long-Term Disability
• 401(k) Retirement Plan
• Competitive salary that is commiserate with experience

• Manages all clinical aspects of study under oversight of the Associate Director of Clinical Affairs including but not limited to initial operational feasibility, study timelines, budget and metrics, and study document development and review (e.g., site training documentation, Informed Consent forms, study-specific plans, and electronic/paper Case Report Forms guidelines).
• Ensures clinical studies/projects are executed in compliance with the associated study protocol and applicable regulations
• Executes clinical monitoring, site initiation visits and close out visits in adherence to Good Clinical Practices (GCPs) and ensures studies are in compliance with the study protocol, TSN Standard Operating Procedures (SOPs), GCP regulations, study-specific manuals/procedures, and will compose/revise relevant reports as necessary
• Oversees data collection, monitoring, and analysis to ensure data integrity and accuracy
• Implement quality control measures to ensure reliability of study results
• Manages the study submission process to IRBs as appropriate
• Provides study-specific training and delivers TSN guidance to site research staff
• Assists in the conduct and internal review of investigator contracts and payments as necessary
• Works with the study team to strategize on clinical study execution
• Helps to facilitate site selection when appropriate and manages start-up processes toward activation of study sites
• Works to develops relationships with investigators and site staff
• Overseas Trial Management File (TMF) management and reviews TMF documents as necessary
• Manage relationships with external vendors and contractors, ensuring that their deliverables meet study requirements
• Performs other duties/responsibilities as assigned or required