Principal Statistican

Discipline: Biometrics
Job type: Permanent
Contact name: Louise Clark

Contact email: louise.clark@rbwconsulting.com
Contact phone: +44 1293 584 300
Job ref: 26368
Published: about 1 month ago
Expiry date: 19 Mar 2023 11:59

Snr / Principal Statistician – leading biostatistics and programming activities!
Location: UK based, remote
Salary: up to £80k plus benefits and bonus

Looking for an opportunity where your role will be responsible for the leadership of Biostatistics and Programming activities?  Leading on regulatory submissions and working closely with key strategic clients? Do you enjoy translating client’s needs into statistical practice and educating clients in their use of statistics?

Our client a global CRO,  is looking for an experienced Snr / Principal Statistician.  This role will provide a great opportunity to work as A Snr Programme Manager to support and provide in depth knowledge of clinical trials methodology, regulatory requirements, statistics as well as statistical software packages (SAS and R). 

Responsibilities will typically include -

• Clinical development plans and study design,
• Statistical aspects of case report form design
• Reviews study database structures, edit checks and data management coding conventions
• Preparation of statistical analysis plans and data analysis
• Interpretation of data and reporting of results
• Writing of the statistical methods sections of integrated study reports
• Integrated summaries of safety and efficacy
• Researching and applying new statistical procedures as needed
• Supporting responses to regulatory questions on the design of the program
• Participating in proposal defense meetings and providing input for proposals
• Work effectively cross functionally internally within the organisation as well as with clients.

What will your Education and work history typically look like? :
    • M.S. or Ph.D. degree in statistics, biostatistics, or related field
    • 9+ years of relevant experience with M.S. OR 7+ years of relevant experience with Ph.D.
    • Excellent communication and project management skills
    • Experience of leading a regulatory submission
    • Knowledge of CDISC standards

For further information on this role and others please get in touch to arrange a confidential chat +44 (0)1293 364114