Job title: Principal and Senior Statisticians
Salary: Excellent Salaries on offer
Position type: Permanent
Location: South East
Job summary:
This is an extraordinary opportunity to be part of a new outsourcing
business model that will be the only one of its kind in the UK. You will be
part of a ''satellite'' operation with two new offices in the South East
serving the biometric outsourced needs of a global pharmaceutical company.
We are looking for a number of senior and principal statisticians over a
number of therapeutic areas. You will provide clinical trials and
statistical expertise and be responsible for statistical aspects of assigned
clinical trials and other non-standard projects. Your expertise will be key
to the success of this operation
Role and responsibilities:
* Will act as subject matter expert or 'champion' in the field
of statistics and programming
* Contributing to the statistical sections of reports
integrated clinical/statistical reports and manuscripts
* Primary responsibility and/ or accountability for the
statistical analyses, tabulations, graphics and listings of clinical trial
data
* Ability to co-ordinate the production of data displays in an
efficient manner for inclusion in statistical reports
* Ensuring statistical reports meet regulatory and company
standards
* Perform QA on work performed by others
* Performs, presents and interprets data manipulations and
statistical analyses
* Derives statistical conclusions and makes recommendations
based on experimental results
* Liase with functional groups and client to understand and
help define requirements
Qualifications and experience:
* MSc in Medical statistics or related field
* Minimum of 3 years related experience within CRO or
pharmaceutical/clinical trials environment
* Broad understanding of statistical methods within the
context of clinical and/or clinical pharmacology trials
* Broad knowledge of SAS and Unix
* Ability to be flexible with respect to changing priorities
and type of work
* Proven ability to organise workload and complete tasks on
time
* Demonstrated ability to work effectively in team environment
* Ability to complete tasks with minimum supervision
* Experience of working across all phases (1-4) of clinical
trials an advantage
Personal attributes:
* Strong interpersonal skills and ability to communicate
effectively
* Ability to prioritise and manage multiple tasks
* Excellent organisational and analytical skills
* Excellent inter-personal and team work ability
* Excellent communication and presentation skills
* Excellent knowledge of spoken and written English
* Ability to negotiate and influence others across multiple
functional areas
To apply for this role or find out about related opportunities please
contact Jonathan Hart-Smith on 0870 0605268, email at
[log in to unmask] or visit our website at www.ircl.co.uk
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