Dear Allstat,
Please find below the latest Senior Statistician vacancy in Manchester
An exciting new biotechnology company based in the North West has a new reuqirement for a Senior Statistician responsible for all statistical aspects of the design, analysis and reporting of assigned clinical trials. The company is developing pharmaceuticals to prevent scarring and accelerate wound healing.
The successful candidate will be 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:
Essential Experience, Qualifications, Attributes:
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 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.
The project management aspects of analysis and planning of the statistical analyses is essential to maintain and where possible improve on performance.
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.
For further information or to apply for this role send your details to Robert Whyte at James Harvard Pharmaceutical.
Email [log in to unmask] or you can call directly on +44 (0) 20 7922 7117
If this opportunity is not what you are looking for but are actively looking for a contract or permanent position as a Biostatistician or SAS Programmer then call for a confidential discussion.
Kind regards,
Robert Whyte
Consultant ~ Clinical & Biometrics Division
James Harvard Pharmaceutical Ltd
T. 020 7922 7117 M. 07957 190569 F. 020 7922 7101
E: [log in to unmask]
W: www.jamesharvardpharma.com
25 - 27 Wootton Street : Waterloo : London : SE1 8TG
For the latest Statistics and Programming vacancies visit www.jamesharvardpharma.com
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