Clinical Research Coordinator
SI-BONE
π΅ $60k-$70k
πRemote - United States
Please let SI-BONE know you found this job on JobsCollider. Thanks! π
Job highlights
Summary
Join SI-BONE, a leading medical device company, as a Clinical Research Coordinator. You will support clinical studies, ensuring adherence to good clinical practice and quality assurance standards. Responsibilities include overseeing daily operations, preparing invoicing, providing clinical site support, and performing GCP tracking and compliance. The ideal candidate is detail-oriented, organized, a team player, and proficient in Microsoft Office programs. A Bachelor's degree in life sciences and ACRP certification are preferred. SI-BONE offers a competitive salary, bonus, and stock options.
Requirements
- 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
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
- 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
- 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
Preferred Qualifications
- Bachelor's degree in life sciences preferred
- Association of clinical research professional's certification is preferred
Benefits
- Salary range: $60,000- $70,000
- Supplemental pay: bonus and stock
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