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:

A hiring company that offers alternative approaches to pay, performance bonuses, and/or equity in the firm is very attractive to you. You're generally less interested in working for an organization offering only traditional, salary-based compensation, one with limited opportunity to acquire equity in the firm, or one that does not actively promote skill development. In addition, you are more likely to choose a company that offers a variety of internal career options, with defined career paths. You view the learning of new skills and development of your expertise as key to your career advancement. These aspects of an organization may become even more important to you as you progress in your field, and are especially critical if you change career or occupation.

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: