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Principal Biostatistician
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Remote, Canada PHASTAR Full timeOverview: **About Phastar** Phastar brings data to life! We are an award-winning specialist biometrics contract research organization (CRO) that works with pharmaceutical, biotechnology, and medical device companies to provide statistical consulting, analysis and reporting, data management, and data science services. Our unique approach to data analysis,...
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Principal Biostatistician
4 weeks ago
Premier Research is looking for a** Principal Biostatistician** 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 medical innovation that patients are desperate for.
Together, we are Built for BiotechSM.** Join us and build your future here.**
**What you’ll be doing**:
- Prepare statistical sections of protocols, performing sample size and power calculation for studies, and create randomization schedule per study design and relevant specifications
- Review protocols, case report forms (CRFs), data management plans, data specifications and other related study documents
- Develop statistical analysis plans (SAP) in accordance with the protocols and SAS programs to create statistical models and complete statistical analyses
- Support integrated summaries of safety and efficacy (ISS and ISE) for regulatory submissions, independently prepare analysis data specifications, perform quality control of analysis data and TLGs
- Develop SAS programs to create derived variables and analysis data sets and computer programs to generate listings, tables, and graphs using SAS
**What we are searching for**:
- Advanced degree (MS or PhD, or equivalent) in statistics or closely related field
- 4-6 years (or 3-5 years for PhD) of direct experience of clinical trials design and regulatory knowledge and analysis with advanced SAS programming experience
- Ability to effectively communicate with others on the project team and in the department; strong interpersonal communication skills
**Why choose Premier Research?**
- Premier Research is more than a company - it’s a community of people that truly care about one another, about our clients, and about our mission of furthering research to improve the lives of patients in critical need.
- Our cultural anchors - Caring & Empathy, Empowerment, Aspiration, One Team - mirror the flexibility and trust that our team embodies. As a Premier team member, you have the power to make an impact, regardless of job title and location.
- Our dedication to biotech and specialty pharma is unlike any other. We provide our staff with innovative technologies and continuous learning opportunities so that they have the tools they need to be successful.
Because we are transforming life-changing ideas into new medical treatments for a diverse population, we require the perspectives of a diverse staff thinking creatively, challenging ideas, and solving complex problems fearlessly. Through a commitment to diversity, equity, inclusion, and empowerment, we create a community of belonging that welcomes differences, fuels innovation, and better connects us to the patients, physicians, and customers we serve.
- Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status._
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