Biostatistician required in the South East - 12 month contract
Thu 29 Apr 2010 - 23:48
A state of the art international Biopharmaceutical company is seeking a Biostatistician for a 12 month project. This will be based in the south east and will be offering a very attractive hourly rate.
Candidates are required to:
- Participate in study team meetings
- Create statistical text for study concept documents and protocols (study design, endpoints, sample size, methods for analysis)
- Review and approve randomization specifications
- Create statistical analysis plans
- Create templates for tables, listings and graphs
- Review and approve SDF dataset specifications
- Review and approve key study-related documents produced by other functions (e.g. CRFs, Data Management Plans etc)
- Write, test, validate and execute software programs to produce SDF datasets and tables, listings and graphs (statistical analysis outputs) for inclusion within CSRs, ISS / ISE, IBs, INDs, publications and other communications
- Participate in the finalization of protocol deviations and analysis sets
- Create statistical text for CSRs, clinical publications and other communications
- Plan and execute statistical review and QC of CSRs, clinical publications and other communications
- Assist in planning and contribute to compilation of ISS/ISE
- Provide input to and participate in intra-departmental and global Biostatistics meetings
If you are available or know someone who may be please contact Rami Nahim from Real Pharma on 0207 758 7322.
Thanks,
Rami
Candidates are required to:
- Participate in study team meetings
- Create statistical text for study concept documents and protocols (study design, endpoints, sample size, methods for analysis)
- Review and approve randomization specifications
- Create statistical analysis plans
- Create templates for tables, listings and graphs
- Review and approve SDF dataset specifications
- Review and approve key study-related documents produced by other functions (e.g. CRFs, Data Management Plans etc)
- Write, test, validate and execute software programs to produce SDF datasets and tables, listings and graphs (statistical analysis outputs) for inclusion within CSRs, ISS / ISE, IBs, INDs, publications and other communications
- Participate in the finalization of protocol deviations and analysis sets
- Create statistical text for CSRs, clinical publications and other communications
- Plan and execute statistical review and QC of CSRs, clinical publications and other communications
- Assist in planning and contribute to compilation of ISS/ISE
- Provide input to and participate in intra-departmental and global Biostatistics meetings
If you are available or know someone who may be please contact Rami Nahim from Real Pharma on 0207 758 7322.
Thanks,
Rami
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