Call for experts for Clinical Trial Document Redaction eLearning course development

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Signup Deadline: 01-Dec-2023
Starts: 04-Dec-2023
Ends: 26-Feb-2024


We are seeking experienced regulatory affairs professionals with experience in clinical trial documentation and redaction to volunteer as subject-matter experts (SMEs) to help RAPS develop a new eLearning course on mastering document redaction for clinical trials.

The role of a volunteer SME will be to ensure that the course accurately reflects the complexities of document redaction and adheres to global regulatory standards. Your input will be instrumental in shaping the course to teach the practical skills necessary for maintaining patient confidentiality, data integrity, and compliance with international laws and regulations. The ideal volunteer is someone with:

  • Expertise in clinical trial processes, with a focus on document management and redaction.
  • Experience with data privacy laws such as HIPAA, GDPR, and other related regulations.
  • Attention to detail and a commitment to promoting best practices in document redaction.

Volunteers Needed:

5 (5 open slots)

Experience Required:

At least 10 years industry experience

Volunteer Stars:



Roya Zarrinnahad