Role: Consultant Statistician
Department: Statistics
Location: Office-based (strongly preferred) in Chapel Hill, NC (USA) or home-based (East Coast, USA)
Job Type: Permanent, Full time
Position Description:
As a Consultant Statistician, you will provide high-level statistical consultancy to clients: providing advice, guidance and technical expertise for more complex studies. You will support the Director of Biostatistics in providing care and mentorship to junior members of the team, as well as lead and deliver statistical projects.
You will also be involved in business development activities to help expand our US presence. Utilizing your network and statistical expertise, you will identify and work closely with potential clients to establish their statistical requirements and provide a solution to help win new business.
Principal responsibilities include:
* Provide statistical consultancy to pharmaceutical and biotechnology clients on a wide range of statistical issues from sample size calculations to regulatory support
* Support and/or lead business development meetings with new and existing customers
* Manage technical communication with clients
* Deliver and lead assigned studies through all phases of statistical planning and reporting, including writing and review of analysis plans, TFL generation, statistical review of deliverables, and writing and review of statistical methodology documentation
* Provide statistical input to the design and review of development programs, study protocols, and study related documents
* Mentor junior statisticians
* Prepare and deliver training for staff and clients on statistical methodology and principles
Skills and Experience Required:
* Masters or PhD in Statistics or Mathematics
* Extensive experience in methodological biostatistics
* Strong working knowledge of GCP, ICH, FDA and other regulatory guidelines, including direct experience supporting customers with FDA interactions
* Previous involvement in business development activities strongly preferred
* Good SAS programming skills
CROS NT CAREERS
As a global Contract Research Organization (CRO), CROS NT enhances clinical trial outcomes and optimizes vendor oversight with data-driven services and solutions. With over 25 years in business, CROS NT relies on its heritage in data-centric solutions to provide expert biometrics and data science services (data management, biostatistics programming and analysis), medical writing, pharmacovigilance, regulatory consultancy and clinical project management and monitoring. We have offices in Europe, the United States and India.
People are at the heart of CROS NT’s philosophy, which is focused on providing a centre of excellence to its customers, and we believe in empowering our employees to think differently, work creatively and challenge the status quo. At CROS NT, you really can make a difference.
We are committed to providing the very best career development opportunities that encourage you to progress in the direction of your strengths and aspirations, so whether you’re looking to develop your technical expertise, project leadership or line management skills, we work with you to help you achieve your goals.
To apply, please email your CV to [log in to unmask]
Candidates must hold a valid US work permit as we are unable to provide sponsorship
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