Clinical Research Protocol Writer – IRB-Compliant Study Protocol Expansion (Healthcare AI Project)

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