Senior Statistician
Manchester £30,000 - £40,000 + benefits
Based in custom-built facilities in the heart of Manchester's academic and clinical centre, Our Client's talented staff have established the company as a world centre for wound healing pharmaceutical research and development. This location provides speedy and extensive transport routes throughout the country, as well as international access. They are now actively seeking exceptional individuals with the drive and skills to help meet all scientific and commercial goals, with specific emphasis on the need for a Senor Statistician.
You will be an expert statistical consultant responsible for all statistical aspects of the design, analysis and reporting of assigned clinical trials. The role will entail:
* Responsible for all statistical aspects of the design, planning and development of assigned clinical studies. Provision of statistical sections of study synopses and protocols.
* Production of the study analysis plan (to establish statistical methods to be applied and the content and format of the final study report).
* Responsible for analysis and report production for assigned clinical studies. This may involve specification and supervision of work by other statisticians, contractors or CROs, but the Senior Statistician has overall responsibility for quality and timelines.
* Maintain high level of expertise in statistical methodologies. Ensure that the most appropriate methodologies are applied. Ensure all work is carried out in compliance with SOPs, GCP and in accordance with regulatory requirements. Maintain high level of expertise in appropriate areas of SAS programming.
* Contact with customers (Directors, Pre-Clinical and Clinical Departments) in relation to studies. The Senior Statistician has a key project management role in ensuring that quality and time commitments are met according to agreed timelines and inputs to the department. This requires effective prioritisation of workload and compliance with appropriate SOPs.
PRIOR EXPERIENCE & PERSONAL TRAITS:
The position of Senior Statistician can only be filled by a qualified statistician with a minimum MSc in Statistics or a Chartered Statistician with 5 years experience ideally in Phases II and III of the clinical trial process. It is this level of expertise together with a high level of computer literacy which will enable efficient high performance within the role.
The study design and protocol input forms a major part of the role which is a key factor in marrying the companies objectives with statistical relevance to ensure that the budget allowed for the study is used effectively to produce meaningful results - without a high level of statistical expertise it would be very easy to conduct clinical trials which have neither the power nor the significance to prove the objectives of the study.
Production of the final statistical report is the contribution to the Clinical Trial Process which the Senior Statistician is solely responsible for. It is not merely a collection of tables, writing the report requires the ability to collate the information into a sensible and meaningful fashion in a professional format but primarily to interpret and draw statistical conclusions to the summary data and the results of the tests performed.
If you have the required qualifications, skills and experience to succeed in this role, and would like to be an integral part of an empowered work-force, please send your complete CV to [log in to unmask] for consideration.
Kind Regards
Jonny Steel
Recruitment Advisor
QUANTICA search & selection
Tel: 01422 370011
Mob: See business card
http://www.quantica.co.uk
mailto:[log in to unmask]
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