Public Policy, Non-profit, Clinical Research, Business Documents and Publications
Expertise
Clear Communication and Professional Presentation
As a public policy and non-profit professional, I understand the importance of
your written materials for your personal success and your organization's integrity.
They leave lasting impressions on executives, colleagues, stakeholders, and the public.
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Over 10 years of public policy and advocacy experience in Washington, D.C., and a Masters of Public Administration (MPA).
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Over 20 years of marketing and communications writing and editing experience.
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Over 15 years of organization management and strategic planning experience.
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GCP certified for clinical trial regulatory documents and materials.
Contact me for a quote on any project related to the following areas of expertise.
Public Policy:
Domestic & International
Present Your Data and Research with Confidence
Public policy impacts the public at all levels, from local to international. It is essential to communicate your message clearly and accurately to convey the importance of your policy issue.
Policy Issues:
Health (policy, insurance, and delivery systems), Nutrition, Environment, Labor, Education, Human Rights, Civil Rights, Agriculture, Political Economics
Document Types:
Reports, Grants, Journal Articles, Media Articles, PhD Dissertations, and Books
Professional Documents & Publications
Clear Presentation and Document Accuracy
The integrity and reputation of your organization is represented by the written material it produces. Make sure your documents are clear, accurate, and professional.
Document Types:
Annual and Quarterly Reports, Policy Issue Reports, Strategic Plans, Change Management, Organization Development, Event & Meeting Materials, RFPs, RFIs, White Papers, PowerPoint Presentations, Grants, Booklets, Brochures, etc.
Clinical Research
Clear Language and Professional Presentation
Your clinical trial documents should reflect the professionalism and integrity of the medical field and give confidence to the IRB, the PIs, and the subjects.
Clinical Research Regulatory Documents:
Protocol, Informed Consent Form, Investigator's Brochure, Supplemental Materials
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Clear language and professional formatting are essential when submitting materials to local and central IRBs.
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Creating simplified ICFs in plain language is fundamental to improving subject understanding per HHS guidelines.
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Experienced editing can give your materials a professional edge and increase the integrity of your study.
