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| Entreprise: |
GlobalSCS Group Ltd |
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| Intitulé: |
Senior Statistical Programmer |
| Secteur Emploi: |
l'industrie Pharmaceutique |
| Localisation de l'emploi: |
Basel - Suisse |
| Description: |
The Sr. Statistical Programmer’s major activities are as follows: Lead programming activities for a trial, early phase project, indication or publication activities; lead a complex/large project under supervision of a Program Statistician/Group Head. Maintain efficient interfaces with internal and external customers with support of SR management and the Program Statistician. Develop resource plans as required with support of the Group head. Develop and comply with project/study standards and specifications following internal guidelines; make certain that documents and specifications are consistent and comply with company standards by providing input into study protocol, CRF and data structures tables, listings and figures for phase I-IV clinical trials and submission activities. Program, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials and for SCS and SCE with high quality and within milestones. In conclusion with the statistician, develop specifications for analysis datasets, pooled datasets and listings. Support quality control and quality audit of deliverables 9) Maintain records for all assigned projects and archiving of trial/project analysis and associated documentation. Participate in the selection of CROs and supervise the SR trial activities of the CROs. Provide input on process improvement initiatives and participate in nonclinical project activities. |
| Capacités Requises: |
Minimum of a BA/BS or equivalent experience in mathematics, statistics, computer science or life science or related field(s). Fluent English (oral and written) Intermediate knowledge of/experience with SAS software Working knowledge of database design/structures. Good understanding of global clinical trial practices, procedures, methodologies. Good understanding of regulatory requirements relevant to SR(e.g. GCP,ICH) Intermediate knowledge of office tools. At least 4 years experience in a programming role preferably supporting clinical trials/or in the pharmaceutical industry (2 years for Ms Statistics/Computer Science graduates).
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| Langues Requises: |
Anglais-Très Bon |
| Type de Contrat: |
Temps Plein |
| Salaire Annuel: |
Non spécifié |
| Date d'Affichage: |
2008-11-24 |
| Niveau d'Etudes: |
Licence |
| Années d'Expérience: |
5 à 7 Ans |
| Entreprise: |
GlobalSCS Group Ltd |
| Nom: |
GlobalSCS Group Ltd |
| Téléphone: |
+445601919214 |
| Methode de Contact Préférée: |
E-mail |
| Preferred Language of Resume/Application: |
English |
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