Statistical Project Programmer
Major Pharmaceutical Client
£ Excellent Salary + Benefits Package + Extensive Relocation Package + Bonus
Job Summary:
The Statistical Project Programmer provides leadership on statistical software programming solutions and their documentation to Biostatistics in general and on a clinical project as assigned. Takes the lead of the statistical programming team and of the statistical programming strategy on the project assigned.
Accountabilities/Responsibilities:
* Lead the statistical programming activities on a project. Provide direction and focus on programming activities related to analysis and reporting of results on the assigned drug development project.
* Provide expert knowledge to Biostatistics on statistical programming strategies. Assess and clarify requirements, provide statistical programming solutions and ensure their effective implementation.
* Guide statistical programming team members on trial protocol review, CRF development and data structure specifications for clinical trials. Ensure consistency and adherence to available standards.
* Oversee the programming specifications within the project and ensures consistency with the statistical requirements for analysis datasets, pooled datasets, listings, tables, and figures. Assist as appropriate.
* Lead activities on programming, validation and documentation according to the agreed specifications of VADs, pooled datasets, listings, tables, and figures. Ensure that high quality standards, consistency within the project and delivery within agreed time lines are being met. Assist as appropriate.
* Ensure adherence to statistical programming standards, effective use of available standard programs, availability of appropriate documentation and compliance with Standard Operating Procedures.
* Coordinate submission specific programming activities, e.g. electronic submission creation.
* Forecast resource requirements and assign resources according to priorities and need within the project. Communicate changes in resource requirements in a timely manner.
* Assess need for external support and when agreed with line management specify technical and delivery aspects of work order.
* Establish and maintain efficient interfaces with internal and external customers. Ensure effective coordination and communication.
Essential Skills & Capabilities:
* University education or equivalent in Mathematics, Statistics, Computer Science or other analytical field.
* At least 6 years of pharmaceutical industry drug development experience using SAS.
* Expert knowledge of SAS programming language, with SAS/Base, SAS Macro, SAS/Graph, SAS SQL and some SAS/STATS.
* Good knowledge of drug development process in particular on collection, storing, processing and analysis of clinical trial data.
* Good knowledge of English, communicating clearly and effectively in written and oral form in a business environment.
* Well developed planning , organizational and analytic abilities
* Strong interest in establishing and maintaining a respectful and effective working environment.
An excellent opportunity awaits for this fantastic opportunity. Interview times booked and full job specification to review...
For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV to [log in to unmask]
James Carrera
Tel: +44 (0) 207 255 6665
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See us at Stand 17 at PHUSE Manchester
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