Dear Allstat,
Please find below our latest permanent Senior Statistician role below. This
position is working from home full time after an initial training period
with the option to work on-site some of the time if you wish.
Salary is negotiable and dependent on the level of experience and you will
occasionally need to come in for meetings when required.
If this role is of interest to you please send an updated CV to
[log in to unmask] or alternatively you can call me on +44 (0)207
922 7126.
Our clients a major Pharma/CRO are actively looking for a Senior
Statistician to join their growing team full time due to an influx of work.
RESPONSIBILITIES
• The provision of expert statistical input and consultancy to Phase I-IV
global clinical trials and clinical development projects including design of
clinical trials.
• Specification and production of analysis and reporting deliverables
(including integrated summaries)
• Responsible for the quality and timeliness of statistical deliverables.
• As Lead Statistician, to be primarily responsible for all statistical
activities on allocated studies including planning and coordination of
activities for assigned statistical and statistical programming team
members.
ACCOUNTABILITIES
• Quality assurance of statistical deliverables of other Biostatisticians
within the department.
•Provide statistical consultancy with regards to design of clinical
development programs and/or trials.
• Provide statistical input (as appropriate) into study protocol and CRF to
ensure that both documents meet the requirements of the study. Ensure
adherence to standards , relevant regulatory guidelines and the provision of
good statistical practice.
• Author and/or provide input to trial Statistical Analysis Plans. Write
detailed statistical methods according to the requirements of the protocol.
Prepare table, listing and figure shells in conjunction with the Statistical
Programmer(s).
• Program and conduct statistical analyses and provide high-quality
statistical output for inclusion in clinical trial reports.
• Provide expert statistical input to clinical trial reports an/or
publications . Write statistical methods section and review results and
conclusions for appropriate statistical interpretation of results.
• Responsible for quality control of all statistical analysis deliverables
and quality assurance of programming deliverables provided by the
Statistical Programmer(s) for assigned trials and/or projects.
• Maintain up-to-date knowledge on statistical techniques and procedures by
attendance at professional courses and conferences and by ongoing review of
statistical literature.
• Assist in the development of analysis and reporting processes to ensure
operational efficiency of Biostatistics’ function.
• Responsible for the specification, programming and statistical reporting
of integrated summaries, including ISS, ISE, CER and other meta-analytic
techniques.
• Perform budget tracking for assigned trials and alert Head of B&SP to
potential cost overruns/out of scope activities. Ensure project and
resource tracking sheets are accurate and updated as required.
• Provide input into recruitment process including interviewing.
EXPERIENCE AND QUALIFICATIONS
• Minimum of a masters (M.Sc.) or equivalent in Medical Statistics in
conjunction with at good experience in the application of statistics in
clinical trials at a CRO or pharma company.
• Experience in programming and reporting inferential statistical analyses
using SAS.
• Expert knowledge of global clinical trial practices, procedures and
methodologies (including regulatory guidelines relating to biostatistics).
• Experience of project managing (timelines and/or budgets) of statistical
activities.
• Strong oral and written communication skills (including the ability to
communicate statistical concepts and information to non-statisticians)
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