Danna P.
Syneos Health
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WORK HISTORY
@Syneos Health
EDUCATION
Remington College-Baton Rouge Campus
Associate of Science - AS, Computer Science
Western Governors University
Bachelor of Science - BS, Health science
Medvance Institute-Baton Rouge
Technical Diploma, Medical/Clinical Assistant
ABOUT DANNA P.
With over eight years of clinical research experience across CRO and site environments, I am a Clinical Research Associate II with extensive experience supporting Phase II–IV global clinical trials. I specialize in site monitoring, regulatory compliance, informed consent oversight, and ensuring protocol adherence in accordance with ICH-GCP and FDA regulations.I have performed Site Qualification Visits (SQV), Site Initiation Visits (SIV), Interim Monitoring Visits (IMV), and Closeout Visits (COV), while ensuring data integrity, patient safety, and regulatory compliance. My experience includes reviewing informed consent forms, verifying consent documentation, maintaining eTMF and regulatory files, supporting audit and inspection readiness, and collaborating with sponsors, clinical trial managers, and cross-functional study teams.My therapeutic experience includes neuroscience, infectious disease, cardiovascular, metabolic, respiratory, vaccines, ophthalmology, nephrology, pulmonology, and general medicine.I am passionate about contributing to clinical operations, supporting ethical and compliant clinical trial execution, and advancing therapies that improve patient outcomes.
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