Peyton Connell, Mph Email & Phone Number

Wilmington, North Carolina, United States

Oversees and manages independent physicians overseeing clinical trial safety andefficacy data.• Facilitates the drafting and finalization of charters, networking cross-functionalinternally and with Sponsors.• Ensures adherence to study protocols.• Facilitates decision-making regarding the safety of participants in clinical trials.• Interfaces with project teams and Sponsors on study deliverables and timelines.• Organizes and facilitates regional and global meetings.• Adequately tracks subject enrollment status and adverse event reporting.• Reviews project budgets and allocates resources for multiple projects.• Maintains knowledge and understanding of clinical research industry,Pharmacovigilance activities, ICH, NIH, and FDA regulations.

Wilmington, North Carolina, United States

Provided administrative support for global and domestic clinical trials focusing onDSMB.• Assisted with project startup and meeting coordination.• Prepared meeting materials and maintained DSMB databases and project files.• Conducted closeout activities, audits, and collaborated on documentationquality.• Processed expense reports and contracts.

Wilmington, North Carolina, United States

Identified and redacted subject identifiers per local requirements, retrained sites,and escalated reoccurrences to data privacy.• Coordinated the timely review of protocol inquiries, serious, and non-seriousadverse events, diagnostics, and DSMB data; tracked necessary data andgenerated reports for the client, project team, and/or external vendors.

Wilmington, North Carolina, United States

Master Of Public Health - Mph, Epidem

Activities and Societies: Board Member of the Public Health Organization

Bachelor'S Degree, Psychology

Activities and Societies: Gamma Sigma Sigma