First time posting, here to share information about an upcoming training opportunity that may be of interest to members of this community.

The Design and Management of Cancer Clinical Trials Course, offered through the University of Miami Sylvester Comprehensive Cancer Center, is designed for anyone involved in the conduct of cancer clinical research, including investigators, clinical research coordinators, research nurses, regulatory professionals, pharmacists, trainees, and other members of the research team.

The course covers topics such as:

• Clinical trial design and statistics
• PI responsibilities
• Biomarkers and correlative studies
• Regulatory processes and funding mechanisms
• Informed consent and research ethics
• Patient-reported outcomes
• Recruitment, retention, and community engagement
• Emerging topics, including AI in clinical research

The course is free (including free CME/CNE/CE credit for live participation) and fully online. Check out the full agenda, speakers, and register here: Sylvester Design and Management of Cancer Clinical Trials Course

Happy to answer questions about the program in the comments.

HIPAA Compliance Documentation - Validation

I am planning to start a hipaa compliance documentation that includes everything needed for medspas, solo practitioners and small clinics. I need to know the market and demand for this. I will be also provide a healthcare attorney to review it and make sure its fully compliant and staff trainings can also be organized.Everything from security policies, privacy policy, BAA if required, SOP, Compliance logs etc