Terug naar zoeken.SEC Recruitment Ltd - Senior Biostatistician - Belgium
| Arbeidstype: | Permanent |
| Plaats: | Belgium |
| Salaris: | €60000 - €70000 per annum + benefits + company car |
| Talen: | Engels, Frans, Nederlands |
Details van de adverteerder
- Naam:SEC Recruitment Ltd
- Gepost:22-09-2010
- Code:9890SEC/BE/STAT/LYB
Our client is one of the world’s leading pharmaceutical company and is currently seeking a Senior Biostatistician to join their biometrics team in Belgium. For more information please contact Louise Beka
Responsibilities
• Design of clinical trials, beginning with identification of clinical goals, statistical endpoints, planned analysis methodologies, power and sample size calculations and data management procedures
• Analysis of clinical trials, starting with the compilation of detailed analysis plans, programming of validated and accurate analysis generation software, review of results with the management and report writing
• Provide statistical consultation for clinical trial activities of the company
• Management of external contract services required for support of drug development projects.
• Interact with project team to plan and identify goals for individual drug development programs
• Work with the regulatory staff to plan and conduct successful interactions with the FDA to ensure efficient progression of the company drug development programs
• Serve as a member of interdisciplinary teams conducting clinical trials and assembling reports of trial results that meet regulatory requirements
Requirements:
• MSc or PhD in biostatistics preferred, with a strong analytic track record
• At least 5 years experience in biostatistics within a pharmaceutical company
• Experience with general linear models, logistic regression, non-parametric and exact procedures , Bayesian analysis, and study size calculations
• Strong oral and written communication skills, including the ability to convey biostatistical principles to colleagues with varying functional specialties and backgrounds
• Demonstrated ability to recommend plans for research design, particularly in the areas of observational studies of comparative effectiveness and safety
• Strong working knowledge of relevant statistical methodology and experience in SAS
• Strong organizational and prioritization skills, including an ability to handle multiple projects
• Advanced computer skills as well as leadership and decision-making skills
If you are interested in this position, please do contact Louise Beka
Responsibilities
• Design of clinical trials, beginning with identification of clinical goals, statistical endpoints, planned analysis methodologies, power and sample size calculations and data management procedures
• Analysis of clinical trials, starting with the compilation of detailed analysis plans, programming of validated and accurate analysis generation software, review of results with the management and report writing
• Provide statistical consultation for clinical trial activities of the company
• Management of external contract services required for support of drug development projects.
• Interact with project team to plan and identify goals for individual drug development programs
• Work with the regulatory staff to plan and conduct successful interactions with the FDA to ensure efficient progression of the company drug development programs
• Serve as a member of interdisciplinary teams conducting clinical trials and assembling reports of trial results that meet regulatory requirements
Requirements:
• MSc or PhD in biostatistics preferred, with a strong analytic track record
• At least 5 years experience in biostatistics within a pharmaceutical company
• Experience with general linear models, logistic regression, non-parametric and exact procedures , Bayesian analysis, and study size calculations
• Strong oral and written communication skills, including the ability to convey biostatistical principles to colleagues with varying functional specialties and backgrounds
• Demonstrated ability to recommend plans for research design, particularly in the areas of observational studies of comparative effectiveness and safety
• Strong working knowledge of relevant statistical methodology and experience in SAS
• Strong organizational and prioritization skills, including an ability to handle multiple projects
• Advanced computer skills as well as leadership and decision-making skills
If you are interested in this position, please do contact Louise Beka
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