Erin H
Site Services Specialist
Habilidades
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Experiência profissional
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Período integral • 5 yrs 7 mos
Site Services Specialist
Oct 2020 - Apr 2025 • 4 yrs 6 mos
Led end-to-end management of multi-site clinical trial recruitment and retention support services across diverse protocols for global research sponsors. • Strategically placed and managed field staff to ensure high-quality clinical trial support and efficient program execution and delivery. • Collaborated with cross-functional project teams to ensure operational alignment with sponsor goals, providing strategic insights that optimized trial performance. • Created and led the 'Site Services Insights' initiative- a quarterly forum to foster team engagement, knowledge-sharing and best practice exchange, strengthening cross-team collaboration. • Developed custom escalation tracking systems tailored to specific programs, improving communication flow, resolving site challenges faster and streamlining overall program execution. • Monitored key site metrics and delivered real-time adjustments and strategic pivots in trial support to maintain program momentum and effectiveness.
Senior Program Coordinator & WorkLife Advisor
Dec 2018 - Jan 2020 • 1 yr 1 mo
Led project coordination following the acquisition of a major corporate client, ensuring a smooth onboarding process and transition of benefits for new members. • Assessed client needs through structured intake and consultation, delivering tailored support solutions in real time and developing client relationships. • Managed a high-volume queue of client support requests, delivering relevant referrals and resources through in-depth, customized research of internal and external sources. • Delivered full-cycle services efficiently and effectively from intake to resource delivery within a defined time frame.
Clinical Research Coordinator & Community Programs Specialist
University of Minnesota • Período integral
Jul 2015 - Nov 2018 • 3 yrs 4 mos
Lead coordinator and project manager for multiple pediatric clinical research studies. • Managed all aspects of trial operations including participant recruitment, conduction of in-person study visits, regulatory compliance, scheduling, data collection and cross-team communication. • Designed and implemented a new specimen management system aligned with GCP guidelines, improving traceability and storage efficiency. • Built and maintained participant relationships across diverse populations, supporting high retention and engagement rates. • Trained and mentored research staff on protocol-specific SOPs and informed consent procedures to uphold clinical and ethical standards and ensure compliance.