Clinical Research Program Specialist

Job Description: 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. Requirements: 3+ years clinical research experience, or advanced degree with experience working with nurses and physicians Bachelor’s degree, Advanced degree in health science field preferred Knowledge of medical terminology Basic understanding of summary statistics with the ability to interpret data in a meaningful way Agile and able to change direction as needed Ability to identify and solve problems independently. Travel fluency Benefits: Supplemental pay: bonus and stock #J-18808-Ljbffr