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Principal Statistician
4 months ago
Responsibilities:
- Guide internal and client study, project and crossfunctional team meetings efficiently.
- You will line manage statisticians, programmers and any other technical personnel.
- Conduct technical evaluation and offer contributions to clinical trial documents which involves protocols, CRFs, CSRs, etc.
- Supervise crucial client projects/portfolios.
- Assist with study and/or compound level actions advising on study design and statistical problems across phases and therapeutic fields.
- You will uphold study master file documents as well as any other documents that are necessary to be audit ready.
- Form efficient cooperative working relationships with both internal and client team members.
- Other duties may be assigned to this role.
Key Skills and Requirements:
- Educated to an advanced degree level in a statistics, biostatistics or similar discipline.
- At least 6 years of experience working in a pertinent organisation.
- Consciousness of industry and project standards and ICH regulations.
- Communication skills both verbally and in writing.
- Comprehension of clinical drug development procedures, pertinent disease areas, endpoints and various study designs.
- Interpersonal skills with the ability to work well in teams.
- Computer literacy with the capacity to manage using SAS or any other statistical software such as R.
- Able to manage own time and workload, orienting around precise accomplishment of competing deliverables.
- Capable of resolving issues with a high attention to detail.
- Works well in independently.
- Able to handle a portfolio of projects and/or people.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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