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Apply online for the
Principal Statistician/Manager Statistician
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Pharmaceutical industry today.
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Principal Statistician/Manager Statistician : GlaxoSmithKline
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| Job Number |
60226 |
| Employee Type |
Full Time |
| Company Name |
GlaxoSmithKline |
| Location |
Research Triangle Park
North-Carolina
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| Salary (year) |
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| Experience |
2 to 5 Years |
| Start Date |
6/2/2010 |
| Industry |
Pharmaceutical |
| Job Type |
Clinical |
| Relocation |
Not Required |
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| Description |
Basic Qualification
• MSc or PhD in Statistics (or equivalent)
• Extensive experience working as a statistician within a pharmaceutical setting, especially Phases 2-3
• Strong technical and communication skills with the ability to work independently
• Ability to make an impact within a cross-functional team
Details
• Track record of statistical contributions and accomplishments in clinical drug development. Experience with the design, analysis and reporting of clinical studies, as well as contributions to the overall clinical development plan. Experience with regulatory agencies is a plus.
• Demonstrated ability to assume a leadership role, especially in championing innovative statistical designs on a cross-functional team. Simulation skills in SAS, R, and/or Winbugs.
• Strong interpersonal skills and excellent written/oral communication skills. Ability to present statistical concepts to non-technical customers in small and large groups.
• Ability to review / co author protocols, clinical study reports, and integrated summaries. Ability to author reporting & analysis plans. Ability to provide knowledgeable and defensible statistical interpretation with release of headline results, statistical analysis package (SAC), due diligence reports, etc. Ability to perform exploratory analyses.
• Demonstrated ability to collaborate with data managers, statistical programmers, clinical scientists, project management, regulatory, and commercial staff.
• Ability to represent statistics on internal teams, including senior level decision committees, and in interactions with contract research organizations, external advisors and regulatory agencies. Evidence of interactions with senior management is a plus.
• Ability to communicate, influence, and lead in a large complex matrix organization. Ability to self direct, organize workload, prioritize, complete tasks on time, and manage activities of assigned support staff.
• Ability to identify and solve technical problems.
• Software skill requirements include use of SAS; R and/or Winbugs is a plus. |
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| Requirements |
Preferred Qualification
• Experience of protocol development, analysis and reporting of clinical trials, and input to clinical trial publications
• Good understanding of international regulatory processes and experience of regulatory interactions
• Ability to influence colleagues in complex situations and make an impact within a cross-functional team-based environment
• Ability to research or apply new statistical methodologies within a clinical trial setting and to communicate statistical concepts to non-statisticians. |
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| Contact Info |
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