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Seltek Consultants Limited,
25a Hockerill Street,
Bishop's Stortford,
Hertfordshire,
CM232DH
UK
Tel: 01279 657716
Email: sales@seltekconsultants.co.uk
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 We handle many vacancies for experienced Statistician and Biostatisticians. Below you'll find examples of typical jobs.
PRINCIPAL STATISTICIAN |
An excellent opportunity to experience first hand the development of a new biometrics department within a global drug development organisation! As the first statistician to be based in this company's new offices in West Sussex you will have full project management responsibility for biostatistics projects including: the development of statistical analysis plans, financial management, resource planning and timeline management. This will be a 'hands-on' role and you will have involvement in the statistical analysis of clinical trial data and act as the lead statistician on high profile, global studies. You will also have input into clinical research programmes from a statistical perspective. As the department grows you will gain supervisory responsibility for less experienced statisticians within assigned projects. A competitive remuneration package is available including pension, private healthcare, life assurance, 22 days holiday and bonus scheme. Call now for further information on this rare and exciting opportunity!
To be considered for this influential role you will have either a life science degree with a MSc in Statistics or a BSc in Statistics - preferably with a strong medical statistics component. A minimum of four years' postgraduate experience in the application of statistics to clinical trials is essential. You will be proficient in the use of SAS including use of a variety of statistical procedures ie non-parametric analysis, linear and non-linear models, categorical data and survival analysis. Good knowledge of the overall clinical trials process and of its application within clinical development is also required. |
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SENIOR STATISTICIAN |
A reputable drug development organisation is experiencing considerable growth and is looking to increase its biometrics capability with the addition of a Senior Biostatistician based out of its offices in the Home Counties. In this rôle you will be responsible for the project management of statistical aspects of pre-clinical and clinical trials both within the UK and overseas. The training and development of junior members of staff and new recruits will also form part of your rôle and this offers a rare and exciting opportunity to gain supervisory experience and eventually take on line management responsibilities. An exciting opportunity to progress your career within the biometrics field within an organisation offering one of the most promising career development structures within the industry!! There is a competitive remuneration package available including pension, healthcare, life assurance and 24 days holiday.
To be considered for this rôle you will possess an MS degree in statistics or related field and at least four years' relevant experience working within clinical research for either a CRO or pharmaceutical company. Candidates with a PhD and two years' relevant experience will also be considered. Overall you will be a confident communicator with a passion for data analysis and people development. |
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SENIOR BIOSTATISTICIAN |
| Advance your career by joining one of the industry's leading global contract research organisations! This is an excellent opportunity to expand upon existing experience within the field of biostatistics. As Senior Biostatistician you will be responsible for all statistical methodology and statistical plans for clinical studies. In this rôle you will liaise with cross-functional groups to provide statistical support to the production of protocols, development of data management tools and databases and the production of clinical/statistical reports alongside medical writers. Some business development involvement will be required through the provision of input in to proposals and presentations to clients. The successful candidate will have an MS degree in statistics with a minimum of five years clinical experience OR a PhD in statistics with three years clinical experience. A thorough knowledge of regulatory guidelines and ICH GCP is essential as is proficiency with SAS. There is a competitive remuneration package on offer to the right candidate including pension, healthcare, life assurance and 25 days holiday. To hear more about this outstanding opportunity please call us now in confidence. |
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LATEST CLINICAL JOBS
A varied and challenging Clinical Research Associate (CRA) role with a leading, specialist oncology research operation in the UK. This organisation is channeling vast amounts of funding into oncology research and in the last two years alone has been involved in the development of various novel cancer treatments.
With increased funding ... more
One of the top ten clinical research organisation (CRO) is expanding, and is keen to recruit a Senior CRA to join their team in the Netherlands. The role can be office or field based with regular travel to monitoring sites. You will assist in managing large scale clinical trial projects or act as a project manager for small scale projects ensuring on time and on budget performance ... more
This leading CRO is looking to recruit a Project Manager to manage phase IV clinical research projects throughout Europe.
This position has arisen due to expansion, as they have recently won a large number of phase IV proposals.
You will lead the clinical team to ensure on-time, on-budget performance, review and approve regulatory and administrative documents from investigator sites, as well as reviewing CRF’s and SAE reports.
You will also ... more
One of the top ten clinical research organisation (CRO) is expanding, and is keen to recruit a Senior CRA to join their team in Germany...more
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