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I'm a PharmD, Scientific Writer, and Medical Communications Specialist based in Cypress, Texas, creating clear, compliant, and engaging content across clinical research, promotional marketing, consulting, and freelance projects.

About Me

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I am a PharmD and medical communications professional with a strong foundation in clinical research, drug safety, and regulatory writing, combined with a passion for strategic storytelling across scientific and commercial environments. Over the past five years, I have built a career that brings together science, communication, and brand development, producing high-quality and trustworthy content that connects with both expert and general audiences.

In my current role as a Senior Scientific Writer and Informed Consent Editor at Houston Methodist Academic Institute, I lead the development, editing, and regulatory review of informed consent forms, clinical protocols, and grant materials. I specialize in transforming complex research language into content that is clear, compliant, and easy for patients and participants to understand, while ensuring it meets institutional, federal, and global requirements.

My background also includes experience in medical affairs, promotional marketing, and healthcare consulting. I have created peer-reviewed articles, conference abstracts, advisory board materials, and brand-centered messaging across multiple therapeutic areas, including psychiatry, oncology, infectious diseases, dermatology, and rare diseases. I regularly collaborate with key opinion leaders, interdisciplinary teams, and sponsors to produce content that is both informative and engaging, distributed across print, digital, and multimedia platforms.

Whether I am supporting clinical teams with regulatory documentation or developing promotional and educational resources, I bring a team-focused mindset, a focus on clarity, and a strong dedication to quality. My goal is to use science-based communication to promote understanding, build trust, and support better outcomes for healthcare professionals, research teams, and the patients they serve.

“You can make anything by writing.”

C.S. Lewis

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My Services

  • Informed Consent Development
    Editing, harmonizing, and reviewing informed consent forms (ICFs) for clarity, compliance, and readability (6th–8th grade level), aligned with institutional, federal, and global regulatory standards.
  • Regulatory & Clinical Writing
    Writing and reviewing clinical protocols, grant applications, case narratives, abstracts, investigator brochures, and study-related documents with a focus on accuracy and scientific rigor.
  • Medical Communications
    Creating peer-reviewed articles, white papers, literature summaries, advisory board materials, and scientific slide decks across multiple therapeutic areas.
  • Promotional Content Development
    Producing compliant, brand-aligned promotional assets including digital newsletters, infographics, patient-facing materials, and omnichannel marketing content.
  • Freelance Writing & Consulting
    Supporting healthcare agencies and medical communications firms with freelance writing services, including web content, blogs, product FAQs, and client-facing deliverables.
  • Plain Language & Health Literacy Editing
    Translating complex medical and scientific information into plain language for patients and public audiences, with emphasis on accessibility and informed decision-making.
  • Strategic Content Support
    Partnering with interdisciplinary teams, faculty, and sponsors to shape messaging that is engaging, scientifically sound, and audience-appropriate for academic, commercial, or clinical needs.

How I work

I approach every project with a balance of clinical precision and narrative clarity, aiming to bridge the gap between science and understanding. Whether I am developing informed consent forms, peer reviewed manuscripts, or promotional materials, my process begins with listening. I take time to understand the needs of stakeholders, the context of the work, and the audience it is meant to reach.

My writing is guided by evidence based communication and shaped by years of experience in regulatory settings, medical affairs, and collaborative content development. I focus on turning technical, often complex information into content that is clear, compliant, and accessible. This applies whether the audience is a patient considering research participation or a physician reviewing therapeutic insights.

I believe in teamwork and thrive in collaborative environments. I have worked alongside clinical investigators, marketing teams, editorial staff, sponsors, and subject matter experts to make sure every piece of content is accurate, aligned, and meaningful. I bring structure to ambiguity, communicate clearly, and deliver work that is both timely and thoughtful.

My experience in freelance writing and consulting has strengthened my adaptability and awareness of audience needs. From internal education tools to patient summaries and brand focused campaigns, I adjust tone and style to meet the unique goals of each project.

At the core of how I work is a simple goal: to communicate in ways that build trust, improve understanding, and support better outcomes for healthcare teams, researchers, and the people they serve.