'Femi Fajimi

sciencecommunication

  • From “Raw TFLs” to Regulator-Ready Narratives: A Medical Writer’s Walkthrough (Antifungal Case Study) 

    From “Raw TFLs” to Regulator-Ready Narratives: A Medical Writer’s Walkthrough (Antifungal Case Study)  By Femi Fajimi | 10 September 2025  (Educational content. Drug, data, and outputs below are fictional but formatted to mirror real deliverables.)  Introduction  Sometimes, when I am asked to support some freelance writers with their ongoing projects, particularly when it involves reviewing

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  • Medical Writing in Oncology: What Makes It Unique? 

    Medical Writing in Oncology: What Makes It Unique?  By Femi Fajimi | 09 June 2025  Oncology is one of the most complex and rapidly evolving areas in medicine, and medical writing in oncology reflects this complexity. Whether preparing a Clinical Study Report (CSR), protocol, or lay summary, oncology writing demands a deeper understanding of disease

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  • From Numbers to Narrative: Learning to Understand Clinical Data as a Medical Writer 

    From Numbers to Narrative: Learning to Understand Clinical Data as a Medical Writer  By ‘Femi Fajimi | 22 May 2025  One of the most valuable skills I’m developing as a regulatory medical writer is the ability to interpret clinical data clearly and accurately. I’m learning that writing about trial outcomes isn’t just about listing results

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  • Writing the Participant Information Sheet: A Practical Introduction

    Writing the Participant Information Sheet: A Practical Introduction By ‘Femi Fajimi | 15 May 2025 The Participant Information Sheet (PIS) is one of the most important documents a medical writer may help prepare during the early phases of a clinical trial. In plain and respectful language, it explains what the study is about, what participation

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  • Writing for Ethics Committee Submissions: Practical Insights from a Developing Writer

    Writing for Ethics Committee Submissions: Practical Insights from a Developing Writer By ‘Femi Fajimi | May 2025 Writing for ethics committee submissions is a key responsibility in regulatory medical writing. It requires clarity, accuracy, and respect for participant rights. As I continue to build experience in this field, I understand the importance of approaching these

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  • Understanding Protocol Amendments: A Beginner’s Perspective 

    Understanding Protocol Amendments: A Beginner’s Perspective  By ‘Femi Fajimi | 14 May 2025  As I continue developing my skills in regulatory medical writing, I’m learning that clinical trial protocols don’t always remain fixed. In practice, they often need to be revised, and that’s where protocol amendments come in.  Understanding amendments has helped me see how

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