SI-BONE

Clinical Research

• The Clinical Research Program Specialist plays a key role in the lifecycle of SI-BONE’s clinical studies.
• Works with the team to plan, design, and implement clinical research projects.
• Collaborates cross-functionally to gather input from other key departments including regulatory affairs, medical affairs, marketing, and R&D.
• Manages clinical study sites and coordinates activities to ensure overall compliance with the protocol and clinical objectives.
• Conducts clinical site monitoring, both remote and onsite.
• Maintains a high level of professional expertise through reading literature, attending society meetings, and interfacing with physician customers.
• Collaborates with study team to draft materials including case report forms, site presentations, and other documents as applicable.
• Responsible for performing all duties in compliance with all applicable worldwide regulatory requirements as included in the scope of the SI-BONE Quality Manual.