プロフィール詳細

プロジェクトを作成

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Dr. Gabriella G.に依頼

United States

Clinical Protocol Writer, Clinical research professional, GCP and CCRP Certified, Scientific writer, Grant proposal

プロフィール概要

Goal-oriented biomedical research with more than 10 years experience and demonstrated achievement in managing clinical/translational research projects for pharmaceutical companies, institutions and independent research organizations, as well as basic science projects in academic institutions. • Clinical research professional, GCP and CCRP Certified, expert knowledge of regulatory and institutional requirements for clinical and medical research, fully equipped with all the skills, tools and proficiency in best practices in project management techniques, clinical research and more specifically Good Clinical Practices. • Excellent research and data organizational skills, critical assessment of results and data analysis; Aid in the evaluation of problems with workflow, organization, and planning and develops appropriate analytical approaches for research studies.

専門分野

• ★ Vaccine Development
• ★ Clinical Trials
• ★ Oncology
• ☆ Microbiology
• ☆ Drug Development
• ☆ Small Molecule Drug Development
• ☆ Diabetes
• ☆ Obesity
• ☆ Cancer Research
• ☆ Regulatory Writing

サービス

• Writing
• Research
• Data & AI
• Product Development

Writing Clinical Trial Documentation, Technical Writing, Copywriting, Newswriting

Research Market Research, User Research, Meta-Research, Feasibility Study, Fact Checking, Gap Analysis, Gray Literature Search, Systematic Literature Review, Secondary Data Collection

Data & AI Statistical Analysis, Data Visualization, Data Processing, Data Insights

Product Development Formulation, Product Evaluation, Concept Development, Prototyping

職務経験

Clinical Scientist

Inovio Pharmaceuticals

12月 2020 - 現在

学歴

PhD

The University of Messina

9月 2001 - 6月 2004

認定資格

• 認定資格の詳細は未入力です。