Clinical Research Coordinator
SI-BONE is a fast-growing, publicly traded medical device company that is an industry pioneer in minimally invasive sacropelvic solutions. Our mission is to help patients rise up and reach for the stars, and our vision is to work together as the global leader to make sacropelvic conditions universally recognized and effectively treated through innovation, evidence, education, and advocacy.
Clinical Research Coordinator
SI-BONE® is focused on helping patients in one of the most under-served, under-diagnosed, and under-treated areas in orthopedics, the sacroiliac (SI) joint. SI-BONE developed an innovative, patented implant to fuse the SI joint. The iFuse Implant System® provides a less invasive alternative to traditional sacroiliac (SI) joint fusion surgery and has been used in over 90,000 procedures to date.
We are a medical device company that is focused on improving the lives of patients with sacroiliac pelvic conditions. We are looking for people who are passionate about our mission and who are willing to work hard to achieve it. We are also looking for people who are:
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Agile: We work in a fast-paced environment and need to be able to learn and adapt to change quickly.
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Creative: We embrace creativity, and we need people who are not afraid to challenge the status quo.
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Team Players: We roll-up our sleeves and work together as one team to achieve our goals.
General Responsibilities
Supports the clinical team on multiple clinical studies. Acts as a resource to clinical research staff to ensure standards for good clinical practice and quality assurance are adhered to in each study. This position requires a high level of attention to detail across multiple documents and studies.
- Oversees and coordinates daily operations of the clinical research team
- Prepares and reviews monthly clinical invoicing
- Clinical site support for materials request
- Performs GCP tracking and compliance for multiple clinical studies, including payments, and sensitive healthcare information.
- Is proactive in all duties
Specific Responsibilities and Skills:
- Responsible for the Trial Master File (TMF).
- Ensures compliance with SOPs and research protocols by providing ongoing quality control audits of study TMFs.
- Tracks and prepares invoicing of clinical milestone payments for
- Prepares study documents for clinical site visits in a timely
- Assists with IRB and publication
- Follows GCP and GDP to ensure all studies and sites are in compliance with SI- BONE study protocols.
Knowledge, Education and Experience:
- Must be extremely detail
- Being proactive is a must for this
- Organized and efficient, this person should be a true team player with excellent verbal and written communication skills.
- Multi-tasking is required for this position and the ability to prioritize numerous
- Proficient with Microsoft Office programs (i,e., Word, Excel)
- A drive to expand knowledge and improve processes
Expertise and Attributes:
- Bachelor's degree in life sciences preferred
- Association of clinical research professional's certification is preferred
Salary range: $72,000- $80,000. The compensation range for this position is specific to the location and is in good faith what SI-BONE expects to pay for the position taking into account the wide variety of factors that are considered in making compensation decisions, including job-related knowledge; skillset; experience, education and training; certifications; and other relevant business and organizational factors.
Supplemental pay: bonus and stock
There are potential risks associated with the iFuse Implant System. It may not be appropriate for all patients and all patients may not benefit. For additional information on the company or the products including risks and benefits, please visit www.si-bone.com/risks.
We are aware of active recruitment scams using the SI-BONE name, in which individuals pose as our recruiters and post fake remote job openings and make fake job offers on the Internet. Please note, we will never make an offer of employment without conducting multiple rounds of interviews face-to-face using secure video-conferencing technology. We will never ask candidates to cash checks or make a payment in order to be considered for a position. SI-BONE only uses company email addresses, which contain “@si-bone.com” to communicate with candidates.
If you believe you’ve been a victim of a phishing scam, please visit the Cybersecurity & Infrastructure Security Agency at https://www.cisa.gov/be-cyber-smart/report-incident learn how to report it.
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Are you passionate about clinical research and making a difference in patients' lives? SI-BONE, a trailblazer in minimally invasive sacropelvic solutions, is looking for a talented Clinical Research Coordinator to join our dynamic team in Santa Clara, CA. As a Clinical Research Coordinator at SI-BONE, you will play a crucial role in supporting our innovative work focused on one of the most underserved areas in orthopedics – the sacroiliac joint. You'll oversee daily operations of our clinical research team, ensuring adherence to the highest standards of good clinical practice. This is not just a job; it's a mission-driven opportunity to contribute to life-changing medical advancements. Your meticulous attention to detail will be critical as you manage the Trial Master File and coordinate milestone payments across various clinical studies. If you're organized, proactive, and a true team player, you'll thrive in our fast-paced environment where creativity and agility are paramount. Join us as we push the envelope of what's possible in patient care and innovation. Let's work together to help our patients rise up and reach for the stars!
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