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

BudgetL $500 + $150 bonus Job 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 Plan 2) Data Sharing and Dissemination Strategy 3) Ethical Considerations and Patient Privacy 4) Clinical Objectives and Methodology 5) 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 protocol 2) Official Study Protocol Checklist for IRB submission 3) Summary brief of the OrthoAI project Apply tot his job