Si Bone Work Values

Daily Duties at Si Bone:

Clinical trials utilizing an implanted medical device for (SI) Sacro-Iliac joint fusion. Management and monitoring responsibilities for multiple clinical trial sites. Compiled reporting in accordance with established timelines and documentation of work accomplished/strategic plans. Performed training of sites pertaining to protocol, process, GCP/ICH guidelines, IVRS, EDC systems, investigational product accountability and overall study management/procedures. Maintained documentation and data integrity for Central File Management. Created documents such as site worksheets/checklists, monitoring & reporting tools, as well as SOPs related to clinical research.

What they like about Si Bone:

Working for a company with an emphasis on social values and helping society is a clear and important priority for you - a critical factor in who you choose to work for. In contrast to other factors, you place an organization's reputation for fairness and concern for the community above most other aspects of the company. As you search for a new job opportunity, it is usually possible to find out if the company is involved in the community and/or if it is addressing problems and issues in society. Pay special attention to non-profit organizations and those specifically involved in social action. Moreover, speaking with current and former employees should enlighten you to perceptions of the fairness of the company's leaders and the treatment of employees.

Tags

Clinical Research, Management, Protocol, Research, Documentation, Medical, Allergy, Monitoring, Reporting Tools, Cardiology, clinical, trial, gcp, protocol, pharmaceutical, regulatory, medical device, CNS, EDC, contract, remote, CRO

Skills

Clinical Monitoring, Problem Solving, EDC, GCP, SOP Development & Implementation, Subject Recruitment, Team Leadership, Contract Negotiation, Safety Reporting, CTMS

These are some of the questions we asked our climbers about their experiences with Si Bone: