Senior Biostatistician – FSP

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Thermo Fisher Scientific

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Biotechnology • Pharmaceuticals • Science

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

10,000+ employees

Founded 1956

🧬 Biotechnology

💊 Pharmaceuticals

🔬 Science

📋 Description

• Lead full scope of Biostatistics contributions to support the Commercial development (ComDev) functions • Provide scientifically rigorous statistical input for supporting ComDev launch strategy • Partner with clinical stat TA lead and colleagues from ComDev functions • Influence and contribute to ComDev strategy to support product launch and life-cycle management • Collaborate with cross-functional team for governance reviews • Ensure full integration of statistical strategy and quantitative evaluation and interpretation of adhoc analysis results • Coordinate priorities and monitor operations within the responsible areas • Ensure timeliness and quality of deliverables • Develop analysis plan for ad-hoc analysis requests of clinical trial data from Medical Affairs, Health Economic and Outcome Research • Manage cross-function analysis plan review to ensure proper statistical methods are utilized and will deliver the desired outputs • Leads development of TFL shells, including authoring and managing team review • Collaborates closely with Statistical Programmers in the development of ad-hoc analysis specifications, programming, QC and production, as well as other tasks to support analysis requests from CSL commercial development functions • Makes statistical contributions to external publications, including authoring of statistical methods and data interpretation

🎯 Requirements

• M.S. or PhD in Statistics or related field • PhD with 8 years of experience or M.S. with 13 years of experience in drug development • Advanced knowledge and training in applications of statistical methodologies • Ability to collaboratively work in matrix environment and provide statistical expertise in matrix environment • Willing to proactively explore the clinical trial data independently with high-level supervision and effectively communicate with CSL teams • Hands-on experience with data mining analysis • Project management skills to enable meeting deliverable requirements in a timely manner and with high quality • Strong interpersonal and communication skills (verbal and written in English) • Good working knowledge of SAS and/or R • Efficiency with Microsoft Office (Outlook, Word, Excel, and PowerPoint) and SharePoint

🏖️ Benefits

• competitive remuneration • annual incentive plan bonus • healthcare • a range of employee benefits