Biostatistics Director – Global BIOS

🕒 Novembro 5

🌐 Estados Unidos, Canadá – Remoto

🇺🇸 Estados Unidos – Remoto (EUA) 🇨🇦 Canadá – Remoto

🌲 North Carolina – Remoto

🌲 North Carolina – Remote

💵 $134.800 - $375.700 / ano

⏰ Tempo Integral

🔴 Especialista

👔 Diretor

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IQVIA

SiteLinkedInTodas as Vagas

10.000+ funcionários

💼 Consultoria

🏭 Manufatura

📣 Marketing

💰 $1.000.000.000 Post-IPO Debt em 2023-05

Consulting • Manufacturing • Marketing

A IQVIA é líder global em análise de dados e soluções de tecnologia, dedicada a melhorar os desfechos em saúde. A empresa utiliza sua plataforma Connected Intelligence para aproveitar o poder de analytics avançado e inteligência artificial, impulsionando a inovação na área da saúde. A IQVIA foca em diversas frentes, incluindo pesquisa clínica, tecnologia e serviços de consultoria, para solucionar desafios complexos em saúde e acelerar a entrega de novas terapias aos pacientes.

Descrição

• Serve as a thought leader in statistical methodology for clinical trial design • Provide high-level statistical consultancy and guidance to internal and external clients • Specialize in at least one area of statistical leadership and serve as a subject matter expert • Lead the associated statistical leadership work and provide general consulting as needed • Participate in data monitoring committees as a blinded or unblinded statistician • Help write protocol synopses with medical, pharmacokinetic, and operational experts • Contribute occasionally to full protocols and consult on advanced statistical analyses • Publish papers in peer-reviewed journals and perform referee and editor work • Present talks at scientific conferences and participate in invitation-only webinars • Manage people and projects depending on interest • Participate in bid defences • Travel to clients as needed

🎯 Requisitos

• PhD or MSc degree in Statistics, Biostatistics, or related field, along with 11 to 13+ years’ experience within the life-science industry; PhD preferred • Strong knowledge of complex statistical methods that apply to applicable clinical trials • Experience with clinical trial design; adaptive design strongly preferred • Knowledge of regulatory bodies and compliance within the pharmaceutical and CRO space; FDA experience preferred • Strong working knowledge of SAS and CDISC SDTM and ADaM • Ability to effectively manage multiple tasks and projects • Ability to communicate and explain statistics • Experience preparing budgets/proposals and participating in bid defences • Experience publishing papers or presenting talks at scientific conferences and/or in webinars

🏖️ Benefícios

• Interesting and innovative projects • Collaborative and inspirational working environment / atmosphere • Excellent career development and progression opportunities • Work – life balance • Incentive plans, bonuses, and/or other forms of compensation may be offered • Health and welfare and/or other benefits may be offered

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