Description
Contract Statistician
6 months contract
Berkshire CRO
£50-60 pr. hour
ASAP start
Role and responsibilities:
* Develop SAS Programs to produce tabulations, graphics, listings, datasets and statistical analysis of clinical trial data to meet client requirements
* Perform QC on tabulations, graphics, listings, datasets and statistical analysis on work by other team members
* Statistical analysis plan (SAP) and shell development with minimal assistance, as well as performing QC of SAPs
* Review and contribute to relevant documentation (e.g. statistical analysis plans, protocol, CRF)
* Deliver assigned tasks on time, efficiently and to required quality
* Provide effective and timely communication to the line manager and relevant project personnel regarding all aspects of day-to-day work
* Perform, present and interpret data manipulations and statistical analyses
* Derive statistical conclusions and makes recommendations based on results
* Contributes knowledge and expertise to manage the team and the client to ensure study milestones are met, to the right quality
* Ensuring statistical reports meet regulatory and company standards
* Develop knowledge in the use of SAS (e.g. macros, statistical procedures) and other in-house reporting systems
* Develop knowledge in the set-up and use of the reporting environment
* Perform exploratory stats using advanced techniques
Qualifications and experience:
* PhD, MSc (or equivalent) in Medical Statistics or a BSc in Statistics and relevant clinical trials experience
* Proven experience within CRO or pharmaceutical/clinical trials environment
* Understanding of statistical methods within the context of clinical and/or clinical pharmacology trials
* Knowledge of SAS essential
* Considerable hands-on Statistical experience
* Knowledge of different phases and types of clinical trial reporting (e.g. Phase I-IV, Clinical Study Reporting, ISS/ISE including e-sub activities) as well methods used for reimbursement and epidemiology
* Excellent understanding of skills and goals of reporting clinical data
* Broad understanding of statistical methods within the context of clinical and/or clinical pharmacology trials
The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the UK. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.
