Global Trial Optimization Specialist

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🕒 3 dias atrás

🔔 Pennsylvania – Remoto

🔔 Pennsylvania – Remote

⏰ Tempo Integral

🟡 Pleno

🟠 Sênior

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ICON plc

SiteLinkedInTodas as Vagas

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

• Develop strategic patient recruitment and retention recommendations for clinical trial teams • Serve as an expert consultant to project teams needing recruitment and retention support • Manage project scope, objectives, deliverable quality, and assigned project activities • Serve as the primary project contact for Patient Recruitment and Retention programs with sponsors • Select and manage recruitment and retention vendors • Coordinate strategy-related activities with study teams and sponsors to meet project milestones • Monitor current and innovative recruitment trends, vendors, and technologies • Use internal and external intelligence to support and refine project strategies • Support process improvement to maintain organizational quality

🎯 Requisitos

• Bachelor’s Degree, preferably in medicine, pharmacy, nursing, or biological science • At least 3 years of career experience, including 2 years in the conduct of clinical trials • Knowledge of business process analytics and continuous improvement highly preferred • Pharma and/or CRO experience highly preferred • Feasibility experience required • Patient recruitment strategy planning experience at site and country level • Infectious disease clinical research background experience required • Analytical skills and ability to synthesize data and differing points of view • Excellent/superior presentation skills • Ability to work in a fast-paced environment • Ability to negotiate and influence stakeholders • Strong interpersonal and communication skills • Knowledge of and ability to apply GCP/ICH and applicable regulatory guidelines • Proficiency with data analysis and presentation software, Microsoft Word, and Excel • Excellent organizational and problem-solving skills • Effective time management and ability to manage competing priorities • Ability to establish and maintain effective working relationships in a matrix environment • Legally authorized to work in the United States • Must not require now or in the future sponsorship for employment visa status

🏖️ 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 • Reasonable accommodations during the recruitment process