A leading CRO is urgently looking for a Permanent Senior Statistical Programmer in Cambridge and in other locations. In addition to multiple locations, an excellent benefits scheme will be available for the right candidate and we also have multiple start dates on offer.

The role would require the candidate to act as a lead programmer on selected multiple projects, overseeing the programming aspects of clinical trials from design through analysis and reporting.  Also, the candidate will be expected to support the lead statistician or lead programmer on projects, by providing statistical programming support for data summaries and listings, and validation programming support in the production of statistical appendices.  Furthermore, the candidate will be expected to suggest, plan and provide developments to tools and techniques for improving process efficiencies and to represent the Biostatistics department within the company and with interactions with client companies and regulatory agencies, as required.  

If you have the required experience for this position and are eligible to work in the UK then please call Maria Latif immediately on 020 7922 7138 and email your CV to [log in to unmask]

 KEY ACTIVITIES:

- Be familiar with and follow the departmental and company standard operating procedures (SOPs) and 
 working practices (WPs)

-Assist in the training and implementation of departmental procedures for the Biostatistics team

-Serve a lead programmer on selected multiple projects

-Ensure projects are well documented consistent with company SOPs and working practices

-Manage a project team for projects.  This involves conducting team meetings, meeting project
 timelines, assessing resources needed, forecasting and input to budgetary needs.  Ensure that SOPs are being
 followed and that appropriate project documentation is ongoing

-Time management of own and team's time spent on projects

-Interact with the sponsor on programming aspects of the project and present at meetings, as required

-Provide the Project Manager, Biostatistics department and company management with timely, accurate status
 and resourcing reports

-Contribute to and review statistical analysis plans, mainly through table, listing and graph specifications.
Specify the general structure of the analysis database, oversee its development, and ensure completeness for
 use in all programming.  Provide programming support for the development and validation of the analysis 
 database

-Produce statistical appendices, with appropriate documentation

-Validate and review statistical appendices, with appropriate documentation

-Contribute to and review results presented in statistical reports, integrated clinical/statistical reports,
 integrated summaries of safety/efficacy and other documents, as required

-Oversee the Quality Review of the statistical reporting of selected projects

-Mentor members of the department, providing project guidance and SAS® programming advice

-Contribute to departmental documents or policies, input into SOP and WP development and revision, and 
 training of new employees

-Contribute to process improvement and department initiatives

-Contribute to the department recruitment process

-Act as a representative of the department to other divisions

-Assist in bidding and business development activities, as required



 
REQUIRED EXPERIENCE: 

-Strong SAS® programming skills and understanding of database structures

-Good organizational skills across individual projects, managing own and team work loads.
 
-Ability to adapt and adjust to changing priorities.
 
-Excellent written and verbal communication skills.
 
-Ability to work in a multi-disciplinary team setting.
 
-Positive attitude and the ability to work well with others.
 
-Basic knowledge of statistical principles applied to the design and analysis of clinical trials.
 
-Ability to interpret and contribute to company policies.
 
-Excellent problem solving skills.
 
-Demonstrated strong attention to detail.
 


REQUIRED QUALIFICATIONS:


-BSc degree in statistics, computing or related field is desirable.  A person without such qualifications will be considered with good relevant industry and SAS® programming experience in a clinical trial environment.
If you have the required experience for this position and are eligible to work in the UK then please call Maria Latif immediately on 020 7922 7138 and email your CV to [log in to unmask]







 

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