Translating Complex Science
Into Clear, Evidence-Based Communication

Medical Writing • Scientific Communications • Medical Affairs

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Evidence. Story. Strategy.

Medical affairs-ready scientific writing built for claims discipline, fast review cycles, and real-world use.

I translate clinical research, guidelines, and real world evidence into clear, review-ready deliverables for medical affairs, education, and cross-functional clinical teams. Expect disciplined terminology, traceable sourcing, and clean QC.

Target roles: Medical Writer • Scientific Communications • Medical Affairs Content • Medical Editor • Clinical Education Developer

Claims-to-source alignment Guideline + endpoint literacy Field-ready FAQs + decks Publication-style narratives

Training

MMSc (Clinical & Translational Research) + MPH (Public Health)

Execution

5+ years evidence-based clinical content under deadline workflows

Standards

ICMJE · GPP3 · AMA-aligned drafting and review readiness

Verification

Guideline-first synthesis + traceable sourcing (primary literature)

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Core Services

Medical Writing • Scientific Communications • Medical Affairs

Deliverables designed for credibility, review readiness, and real world use. Built with disciplined terminology and source traceability.

Medical Writing

Evidence + Publications

Publication-grade writing that protects scientific intent, claim integrity, and clarity under review.

  • Manuscripts, abstracts, posters, congress summaries
  • Literature reviews, evidence tables, annotated bibliographies
  • Endpoints and safety/efficacy framing with appropriate limitations
  • QC: claims-to-source checks, terminology consistency, version discipline

Scientific Communications

Education + Clarity

Audience-specific communication for clinicians, learners, and cross-functional stakeholders that is accurate and usable.

  • Teaching decks, training resources, internal education
  • CME/CE outlines, learning objectives, facilitator notes
  • Guideline summaries and therapeutic landscape briefs
  • Data-to-slide narrative structuring for rapid review

Medical Affairs Support

Strategy + Enablement

Modular tools that support scientific exchange, internal alignment, and field readiness.

  • Scientific platforms, core claims, key messages
  • FAQs, briefing documents, advisory board materials
  • Slide narratives, Q&A preparation, insight-ready summaries
  • Review cycle support with templates and clean handoffs

Workflow

A Quality System Built for Medical Review

A repeatable process that keeps scope, sources, and stakeholders aligned and supports efficient review cycles with defensible outputs.

1) Define the Use Case

Audience + intent

Align audience, channel, and decision point so the deliverable is clinically relevant and appropriately technical.

  • Scope, outline, success criteria, and review pathway
  • Terminology rules and definitions control
  • Reference plan and claims expectations

2) Extract and Structure Evidence

Traceability

Build from source materials first, then draft with citation discipline and consistent terminology.

  • Study design, endpoints, limitations, applicability
  • Claims framing and reference alignment
  • Clean narrative structure for fast SME review

3) Review, QC, Handoff

Submission ready

Iteration with tracked changes, version control, and QC that protects accuracy and audience intent.

  • Feedback reconciliation and decision logging
  • Consistency checks across modules and slides
  • Final clean files and traceable source trail

Credentials

Academic Training and Scientific Rigor

Interdisciplinary training supporting evidence accuracy, clinical relevance, and high-impact medical communication across research, education, and operations.

Education

Degrees

  • MMSc, Clinical & Translational Research, Medical College of Wisconsin
  • MPH, Public Health Studies, Indiana University Fairbanks School of Public Health
  • BS, Biology & Life Sciences Communication, University of Wisconsin–Madison

Clinical Domains

Depth + agility

  • Primary depth: Psychiatry · Neuroscience · Addiction Science
  • Clinical systems: Emergency medicine · Population health
  • Evidence themes: Infectious disease · Dermatology · Cardiology · Oncology
  • Approach: guideline-first synthesis and clinically grounded framing

Methods and Tools

Standards + execution

  • ICMJE · GPP3 · AMA style alignment
  • Evidence appraisal · data interpretation · claims discipline
  • EndNote/Zotero · Track Changes · version control
  • Medical review workflows including Veeva Vault when applicable
Quamaine C. Bond headshot

Quamaine C. Bond, MMSc, MPH

Medical Writing • Scientific Communications • Medical Affairs

I am a medical affairs and scientific communications professional with advanced training in clinical and translational research and public health. I translate complex evidence into clear, audience-appropriate deliverables that move smoothly through review.

I partner closely with physician SMEs and cross-functional stakeholders to preserve scientific intent while improving structure, clarity, and usability. This includes disciplined terminology, traceable sourcing, and reliable execution in remote, deadline-driven workflows.

CV Highlights (Web Summary)

  • Claims discipline and reference verification (guidelines + primary literature)
  • Clinical narratives, publication-style writing, evidence summaries
  • Case-based vignettes, Q&A, rationales, rubrics, scoring anchors
  • SME reconciliation, action tracking, version control, clean handoffs
  • Medical affairs enablement: FAQs, briefing docs, advisory board materials
  • Bias-aware, patient-safe language and health literacy optimization
  • Therapy-area agility using structured evidence mapping
  • Tools: Word (Track Changes), PowerPoint, Acrobat, Zotero/EndNote

Get in Touch

Clear, evidence-based communication for healthcare teams.

Share your deliverable type, target audience, and timeline. I will follow up with next steps, scope options, and a clean path to a review-ready draft.