Senior Director, Biostatistical Science
Premier Research is looking for a Senior Director, Biostatistical Science to join our Biostatistics team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. We are Built for You.
We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. We are Built by You.
Your ideas influence the way we work, and your voice matters here. We are Built with You.
As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Together, we are Built for Biotech.
Join us and build your future here. What you will be doing: Ability to manage, coach and mentor others and de-escalate difficult situations with clients, teams, and management. Demonstrated critical thinking with a history of bringing forward strategic initiatives and ability to lead process improvement efforts. Acts as project manager for biostatistics stand-alone work and provides internal consultancy to team members (internal/external to Biostatistics) on statistical issues. Provides consultancy to sponsors on statistical issues. Leads cross-functional initiatives/effective change management of process or technical improvements that improve operations and department standards practices. Contributes to the definition of standards and harmonized procedures across offices/regions by developing templates and guidelines as well as training materials. What we are searching for: Advanced degree (MS or PhD) from accredited college or university, in statistics or closely related field. Equivalent combination of education, training and experience will be considered. 15+ years’ experience in clinical trials design and analysis, preferably in a CRO environment. 5+ years in a technical leadership role. Excellent demonstrated working knowledge of advanced clinical trial design and analysis principles. Excellent working knowledge of CDISC standards and application of these standards to projects.
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Premier Research is looking for a Senior Director, Biostatistical Science to join our Biostatistics team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. We are Built for You.
We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. We are Built by You.
Your ideas influence the way we work, and your voice matters here. We are Built with You.
As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Together, we are Built for Biotech.
Join us and build your future here. What you will be doing: Ability to manage, coach and mentor others and de-escalate difficult situations with clients, teams, and management. Demonstrated critical thinking with a history of bringing forward strategic initiatives and ability to lead process improvement efforts. Acts as project manager for biostatistics stand-alone work and provides internal consultancy to team members (internal/external to Biostatistics) on statistical issues. Provides consultancy to sponsors on statistical issues. Leads cross-functional initiatives/effective change management of process or technical improvements that improve operations and department standards practices. Contributes to the definition of standards and harmonized procedures across offices/regions by developing templates and guidelines as well as training materials. What we are searching for: Advanced degree (MS or PhD) from accredited college or university, in statistics or closely related field. Equivalent combination of education, training and experience will be considered. 15+ years’ experience in clinical trials design and analysis, preferably in a CRO environment. 5+ years in a technical leadership role. Excellent demonstrated working knowledge of advanced clinical trial design and analysis principles. Excellent working knowledge of CDISC standards and application of these standards to projects.
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