Job Description
BudgetL $500 + $150 bonusJob Description:We are seeking a highly experienced and detail-oriented professional to assist in the expansion and refinement of a clinical research study protocol for submission to an Institutional Review Board (IRB). The project is part of OrthoAI, a multidisciplinary AI-in-healthcare research initiative focused on orthodontics and diagnostic decision support.Scope of Work:- Review the current draft of our IRB study protocol.- Align the document with the official IRB Study Protocol Checklist.- Expand key sections to ensure regulatory, clinical, and data protection compliance.- Integrate elaborated content for areas such as:1) Data Retention and Storage Plan2) Data Sharing and Dissemination Strategy3) Ethical Considerations and Patient Privacy4) Clinical Objectives and Methodology5) Study Design, Timeline, and Risk-Benefit Analysis- Ensure the document reflects best practices in biomedical/clinical AI research protocols.- Collaborate with our internal team (project lead and principal investigators) and iterate based on feedback.
Qualifications:- Proven experience drafting IRB-compliant study protocols, preferably in healthcare or clinical AI domains.- Strong understanding of research ethics, data protection, and academic writing standards.- Familiarity with GCC or international IRB practices is a plus.- Master’s or PhD in Clinical Research, Public Health, Biomedical Sciences, or related field preferred.Deliverables:- A polished and expanded version of the IRB study protocol ready for submission.- Incorporation of all checklist elements provided.- Completed within a 7 day timeframe (negotiable depending on availability).- Attachments (will be provided to shortlisted candidates):1) Current draft of the IRB study protocol2) Official Study Protocol Checklist for IRB submission3) Summary brief of the OrthoAI project Apply tot his job
Ready to Apply?
Don't miss out on this amazing opportunity!
🚀
Apply Now