Director of Statistics and Programming
- Employer
- RBW Consulting
- Location
- Oxfordshire (GB)
- Salary
- £75,000+
- Start date
- 11 Oct 2019
- Closing date
- 10 Nov 2019
View more
- Discipline
- Data Management / Statistics, Biostatistics, Clinical Data Management, SAS Programming, Statistical Programming, Statistics
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Director/Executive
Job Details
Director of Statistics and Programming
How would you like to be a driving force behind the growth and expansion plans of an up and coming Oncology focused research company, My client are expanding and their first plan is to hire a Director of Statistics and Programming to lead the Biometrics functions,
You will be part of a small organisation that focus predominantly on building and adapting products to efficiently target specific forms of Cancer,
Responsibilities Include:
·Acts as the primary contact for and oversees all statistics & Programming activities performed by CROs and vendors
·Acts as the responsible for all statistical aspects including trial design, programming, analysis and regulatory filing strategy.
·Work with external vendors to create eCRFs and study databases, statistical analysis plans and statistical outputs.
·Support the development of data transfer agreements and specifications with various vendors
·Provides statistical input and support to Regulatory submissions
·Create and review SOPs in accordance with current GCP and ICH guidelines
Minimum Requirements:
·MSc/PhD in statistical science
·A minimum of 5 years clinical oncology experience in biostatistics in a pharma or CRO company
·Candidates must be fluent in English language and have excellent communications skills
·Strong project management
·Experience in people management and CRO management is desirable;
·Comprehensive knowledge of statistical theory and methods and demonstrated ability to apply it to all phases of clinical trials.
·Expertise in SAS programming including statistical analysis, data manipulation and scientific graphing. Other clinical software (e.g. R) are desirable.
· data standard requirement CDISC experience
·EDC is desirable
·Strong understanding of clinical trial data and GCP requirement
My client is looking to speak with individuals who have a passion for science and a motivation to walk hand in hand with them in the pursuit to revolutionise Oncology detection methods
My client is looking to speak with individuals who have a passion for science and a motivation to walk hand in hand with them in the pursuit to revolutionise the way we understand and interpret data through complex simulation models,
Get in touch today for further Information!
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