Kennedy Cantrell
Clinical Research Professional | Site Specialist II at ICON plc | Feasibility, Start-up and Activation
- Role
- Site Specialist Ii at ICON plc
- Location
- Charleston, SC, US
- LinkedIn followers
- 500 followers
About Kennedy Cantrell
Regulatory Specialist and Clinical Research Professional with progressive experience managing oncology, pulmonary, and behavioral health clinical trials from start-up through closeout. Skilled in IRB submissions, multi-site project coordination, participant recruitment, and audit-ready documentation, with a proven ability to streamline workflows and ensure compliance with GCP and institutional guidelines. Experienced in liaising with sponsors, CROs, investigators, and community stakeholders to successfully implement complex protocols. Strong background in data management, regulatory oversight, and longitudinal study execution, complemented by leadership, teaching, and community engagement experience. Certified in CITI and ACRP, with proficiency in clinical trial management systems.
Experience
Site Specialist Ii
Feb 2026 — Present
Support preparation, process and tracking of regulatory and site level critical documents and of site activation tasks required for study site activation in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable regulations/guidelines and the principles of ICH/GCPEmbrace and contribute to ICON’s culture of quality and process improvement with a focus on enhancing processes, systems and tools, adding value to our business and meeting or exceeding client needs.
Education
College of Charleston
Public Health B.S.
2017 — 2021
College of Charleston
History
2017 — 2021
LSU Shreveport
Master's degree, Heath Administration
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