プロフィール詳細

プロジェクトを作成

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Kelly B.に依頼

United States

Clinical & Regulatory Document Specialist | Informed Consent, IRB Submissions, Proofreading & Plain Language Editing

プロフィール概要

I am a clinical and regulatory specialist with over 20 years of experience improving the clarity, accuracy, and usability of clinical research documents, including informed consent forms and study materials.

専門分野

• ☆ Clinical Trials
• ☆ IRB Applications
• ☆ Clinical Trial Design
• ☆ Patient Recruitment
• ☆ Regulatory Affairs

サービス

• Writing
• Research
• Consulting

Writing Clinical Trial Documentation, Medical Writing, Non-Medical Regulatory Writing

Research Fact Checking, Gap Analysis, Scientific and Technical Research

Consulting Healthcare Consulting, Regulatory Consulting

職務経験

Regulatory Affairs Principal

NMDP

8月 2022 - 現在

Regulatory Affairs Specialist

National Cancer Institute, National Institutes of Health

4月 2004 - 8月 2022

学歴

Nursing

Towson University

8月 1998 - 5月 2002

認定資格

• Registered Nurse

  Maryland

  8月 2002 - 現在