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 Now
Apply Now
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 Now
Apply Now