Write for us: About Clinical Trial Solutions

Write for betterclinical
as a Guest Contributor.

Would you like to showcase your knowledge to our audience?

Write for us about clinical trial solutions

We’re looking for those who work with clinical trial software, clinical trial solutions & technologies to share what they’ve learned and what they know with our community.

If you’ve found useful approaches to common challenges, discovered efficient workflows, or have insights on specific tools (CTMS, eTMF, EDC, ePRO, Ai tools, etc), we’d love to hear from you.

Our readers appreciate practical information they can apply to their own work.

Whether you’re an author, industry professional, software vendor, CRO, biotech or pharmaceutical company, clinical researcher, project manager, developer or someone associated with the clinical research, clinical trial and regulatory sector, your real-world experience matters. No need for polished perfection, just honest insights that could help others in the field.

If you’re interested, contact us with a brief overview of what you’d like to write about.

Benefits to you

Here’s a summary of how you can benefit from becoming a contributor.

  • Targeted Audience: Share your expertise with readers in your niche; life sciences companies involved in clinical research and clinical trials
  • Ability to showcase your thought leadership
  • Subtly promote your brand/business
  • Gain valuable backlinks to your site.

What content should you contribute?

AI-generated content is everywhere, and we’re careful about what we publish and share with our audience. We want the content we publish to be helpful for our readers. The majority of them are active buyers looking for tolls, software and solutions to help with their clinical trial needs.

Our readers are particularly interested in:

  • Articles
  • How-to guides
  • Vendor selection process
  • Practical advice
  • Case studies
  • Summaries of Industry research reports
  • Industry information
  • Opinion pieces

Topics can be related to any of these:

  • Clinical Trial Management System
  • eTMF Software
  • EDC Software
  • ePRO software
  • Clinical Statistics software
  • Drug Regulatory Software
  • Clinical Trial Project management software
  • Clinical Trial financial software
  • AI technologies for clinical trials
  • Remote clinical trial technologies
  • Clinical Data Management Systems
  • eCRF
  • eCTD
  • Clinical Trial Application software
  • Randomization & Trial Supply
  • Overall clinical trial solutions

We will provide further guidelines to those accepted as guest contributors.

Please contact us if you require further information before proceeding. 

Please fill out all fields and provide a detailed message.

Single article contributors may need to reapply later if they decide to contribute on an ongoing basis.
You must be listed as the author. If more than 3 links are submitted, only the first 3 will be considered.
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