Apply for this job

For more information speak to Jake Akale on 01727 817 620

To apply by email

Apply Now


Salary:£60000 - £90000 per annum

Added:12 Oct 2017

Region: Europe

Sector: Pharmaceutical

Sub Sector: Statistics

Responsible for all biostatistical aspects of the project and/or trial, the statistician Informs and suggests solutions to the statistics head on critical issues within the project Discusses protocol and CRF with the authors and members of the clinical team/clinical trial team. Writes or supervises the writing of the statistical section of the protocol. Verifies the consistency of the protocol with the CRF. Ensures that the trial design is compatible with the trial objectives. Writes or supports the writing of the statistical section/module of reports (FSR, integrated safety/efficacy reports and publications). Reviews and approves the reports. Verifies adherence to statistical standards and SOPs within the project. Performs role of mentor for statisticians, statistical programmers and trainees. Maintain / develop a high standard of statistical methodology.

Apply Now Back To Jobs

We can support your employee requirements

Speak with our support team on 01727 811 634

Contact Us