General Responsibilities:
- Plays a key role in the lifecycle of SI-BONE’s clinical studies.
- Collaborates cross functionally to gather input from other key departments.
- Manages clinical study sites and coordinates activities to ensure overall compliance.
Specific Responsibilities and Skills:
- Conducts site qualification, initiation, interim monitoring, and close out visits.
- Trains sites on protocol, process, systems, and study management.
- Collects and maintains site essential documents.
Knowledge, Education, and Experience:
- Knowledge of medical terminology.
- Agile and able to change direction as needed.
- 3+ years clinical research experience.
SI-BONE
SI-BONE is a medical device company focused on minimally invasive sacropelvic solutions. They aim to help patients with sacroiliac pelvic conditions and have provided over 90,000 procedures to date using their iFuse Implant System.