Responsibilities:
- Lead end-to-end execution of clinical studies, including project management, site management, and study data leadership.
- Perform site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance and data quality.
- Manage essential regulatory and study documents, keeping them complete, accurate, and audit-ready.
Collaboration:
- Collaborate with the clinical team and cross-functionally with Regulatory, Medical Affairs, and R&D to support study planning and execution.
- Maintain strong relationships with investigative sites and physician partners to align with clinical and business objectives.
Qualifications:
- Bachelor’s degree with 4+ years of clinical research experience; advanced degree in health science is preferred.
- Knowledge of medical terminology, applicable regulations, and clinical best practices.
- Excellent verbal and written communication skills, with a friendly, outgoing personality to build trust with surgeons and coordinators.
SI-BONE
SI-BONE is a publicly traded medical device company pioneering minimally invasive sacropelvic solutions. It is a fast-growing organization focused on innovation and evidence-based treatments.