Alice Arnold
Sr Clinical Trial Assistant @ICON plc
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WORK HISTORY
Sr Clinical Trial Assistant @ICON plc
US
Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.*Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.*Support the preparation of study-related materials, such as informed consent forms and case report forms.*Work with cross-functional teams to facilitate communication and ensure smooth trial execution.*Contribute to the tracking and reporting of clinical trial metrics and milestones.
EDUCATION
Faulkner University
Associate of Science - Secretarial Management and Computer Business Applications, Business Administration and Management, General
University of North Alabama
Bachelor’s Degree Office Administration, Business Administration and Management, General
ABOUT ALICE ARNOLD
I’ve built my career on ensuring that every trial begins with a solid foundation of accurate feasibility assessments, reliable sites, and fully compliant documentation. I specialize in site identification, CDA negotiation, and regulatory coordination, bringing both precision and partnership to every study I support. My work has spanned a wide range of therapeutic areas and has included collaboration with leading global sponsors and CROs to accelerate study startup and strengthen operational readiness.At Syneos Health, I’ve led site feasibility and activation efforts across the US and Canada, negotiated dozens of master CDAs, and maintained an impeccable audit record through disciplined adherence to GCP and ICH guidelines. My approach blends data-driven decision-making with relationship-building, ensuring that investigators, sponsors, and regulatory teams remain aligned from the earliest stages of study activation. I take pride in mentoring new specialists, sharing best practices, and helping teams work efficiently within systems like Veeva Vault, PRISM, and Vault Clinical.I’m passionate about supporting high-quality clinical research that advances patient care and scientific discovery. If you’re seeking a trusted partner to drive compliant, efficient study activation or strengthen site identification processes, let’s connect to explore how I can help your organization achieve its research goals.
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