Site Selection Lead

🕒 5 dias atrás

🇺🇸 Estados Unidos – Remoto (EUA)

⏰ Tempo Integral

🟠 Sênior

🗣️🇺🇸🇬🇧 Inglês obrigatório

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Logo of ICON plc

ICON plc

10.000+ funcionários

Fundada em 1990

💼 Consultoria

🏥 Saúde

📦 Logística

Consulting • Healthcare • Logistics

A ICON plc é uma provedora global de serviços clínicos, de consultoria e comerciais que atendem a diversos setores das indústrias de saúde e farmacêutica. A empresa oferece uma ampla gama de soluções clínicas, incluindo ensaios clínicos descentralizados, soluções de segurança cardíaca, laboratórios clínicos de fases iniciais e imagem médica. A ICON também fornece soluções de tecnologia que apoiam o desenvolvimento de medicamentos desde as fases iniciais até o pós-comercialização. Sua expertise terapêutica abrange cardiovascular, oncologia, medicina interna e mais, com forte foco em terapias transformadoras, como terapias celulares e gênicas e biossimilares. Reconhecida como uma das principais CROs (Contract Research Organisations), a ICON oferece regularmente thought leadership e contribui para publicações e eventos do setor. Seus serviços são personalizados para otimizar ensaios clínicos, fornecer inteligência regulatória e gerar evidências do mundo real por meio de análise de dados robusta e soluções centradas no paciente.

Descrição

• Serve as the primary point of contact for all site selection activities across assigned clinical studies • Lead end-to-end site selection strategy with cross-functional teams, sponsors, and country feasibility managers • Develop and implement protocol-specific site selection criteria, site profiles, questionnaires, ranking methodologies, and recruitment strategies • Collaborate with Study Start-Up and Project Management teams to deliver site activation milestones, including FPI, on time and within budget • Oversee site outreach activities, including leadership, training, performance management, and mentorship for site selection team members • Conduct site due diligence, feasibility assessments, and risk evaluations • Monitor study budgets, timelines, resource utilization, and key performance metrics • Track, report, and provide strategic recommendations to sponsors and project teams • Maintain accurate and complete feasibility, recruitment, and site selection documentation in applicable systems • Prepare and deliver client presentations, support business development efforts, and provide strategic expertise on site and country selection planning • Travel approximately 15% domestically and/or internationally

🎯 Requisitos

• 5+ years of site selection and/or feasibility experience at a clinical research site, CRO, or sponsor company • Ability to interpret clinical trial protocols and translate study requirements into site selection criteria, feasibility assessments, and site-specific operational needs • Strong understanding of ICH-GCP guidelines, FDA/EMA regulations, and clinical research requirements • Strong analytical and critical thinking skills evaluating site performance, feasibility data, and recruitment projections • Exceptional verbal and written communication skills • Ability to present recommendations and build relationships with sponsors, investigators, and internal stakeholders • Bachelor's degree in life sciences or another related field • Legal right to work in the United States

🏖️ Benefícios

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways

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