Biostatistics Director – Global BIOS

🕒 3 days ago

🌐 United States, Canada – Remote

🇺🇸 United States – Remote 🇨🇦 Canada – Remote

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $134.8k - $375.7k / year

⏰ Full Time

🔴 Lead

👔 Director

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• 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

🎯 Requirements

• 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

🏖️ Benefits

• 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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