Clinical Research Program Specialist
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Job Description
Clinical Research Program Specialist at SI-BONE managing clinical studies lifecycle and collaborating cross-functionally with various departments.
Responsibilities:
- 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
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