Dear all,
Please find below the latest permanent opportunities for SAS programmers and Biostatisticians:
SAS programmers/ Senior SAS programmer
Permanent role
Client: CRO company
Location : Germany
Very competitive salary package
Responsibilities:
To support the generation and review of the procedures, guidelines, manuals and/or other documents applicable to the general or project-related biostatistical activities. Specifically, to generate, evaluate and validate SAS programmes as required within the evaluation process. This also includes to perform plausibility checks and other quality control actions in biostatistical areas, and to generate tables, lists, diagrams and other data presentation tools as requested by sponsor and/or company directives.
To report to the line manager on the biostatistical activities. This activity includes to generate, review, update, submit and archive these reports as required.
If requested, to support the creation of a biostatistical team, as well as the set-up and evaluation of the methodology applicable to each project. Additionally, to support the control of timelines of each project, and to implement actions in case of problems.
Requirements:
Degree in Medical Statistics or equivalent Experience with SAS and other statistical software Experience in the statistics area clinical trials or equivalent experience Organised, methodical approach Good analytical skills Knowledge and appreciation of statistical requirements of regulatory agencies and ICH-guidelines
SAS programmer
Permanent role
Client : Pharma company
Location : France
Great salary+benefits
Responsibilities:
Responsible for all implementation in SAS of any outputs of the clinical reports.
Collaborate closely with the project programmer to implement template programs Participate in the blinded report planning meeting (BRPM).
Together with the Trial Statistician, the TPROG is responsible for the Mock Report SAS implementation, including the Analysis datasets, tables, graphs and listings and according to the TSAP specification
Key requirements for the position:
SAS programmer should have a very good SAS V9 experience with at least 3 years in Clinical report SAS implementation
Senior SAS programmer
Permanent position
Client: Pharma company
Location: Germany
Excellent salary package
Responsibilities:
Program analysis datasets, pooled datasets, listings, summaries, figures and tables for phase I-IV clinical trials and for overall summaries of safety and efficacy
Provide input as appropriate into specifications for data listings, data summaries/tables and figures for phase I-IV clinical trials
Provide input from a statistical programming perspective to the statistical analysis plan, the QC plan and project convention documents
Experience and Qualifications :
Minimum of BSc/BA or equivalent in computer science, mathematics, statistics, life sciences or related field(s)
Excellent SAS programming skills (BASE, MACRO, GRAPH)
Knowledge and experience in database design and structures
Knowledge of clinical trial practices, procedures and methodologies
Good knowledge of statistical principals underlying clinical trials
Senior Biostatistician
Permanent position
Client : Pharma company
Location: Germany
Excellent salary package
Responsibilities:
-Providing statistical input at the clinical project and trial level in alignment with the overall clinical strategy
- Applying "state-of-the-art" statistical modelling, simulation, predictions and analysis methods for optimizing trial designs and clinical development programs
- Writing statistical plan, conducting data analyzes, interpreting, presenting and reporting statistical results
- Looking for opportunities for applying innovative statistics to research and development of new drugs
- Providing input to the clinical part of regulatory documents and representing statistics at regulatory authorities and in the scientific community
- Working according to ICH-GCP and ICH-biostatistics guidelines
Qualifications:
- Experience in biostatistics in the pharmaceutical industry within a fast paced, change driven and international environment
- You have a University degree in mathematics/statistics, biometry or equivalent degree
- You have experience at interacting with very senior levels and effective at interacting with all levels of employees across highly matrixes organization
If you have the skills and experience for this opportunity please email your C.V. to [log in to unmask] or call +44(0)1273 727 930 for further details.
Andrea is a Biometrics expert at Stelfox Pharmaceutical Search covering Europe, UK, North America and Asia.
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