inVentiv Health Clinical (formerly known as Pharmanet i3) is currently recruiting for two positions working through our staffing division, based at our client site in Surrey.
You will be working within a leading Pharmaceutical and Consumer company, and these are excellent opportunities to work both at a technical and project level within clinical trials.
The positions are full time and office based in Surrey, UK and can be offered either as a freelance contract for 12 months (renewable), or through a permananent contract of employment.
Excellent rates of pay or a competitive salary (plus benefits) are on offer for candidates with the right experience.
Senior Statistician
Working as Senior Statistician, your responsibilities will primarily be as follows:
Provide scientific statistical input to development plans and to project planning.
Provide representation on project teams
Make study design recommendations and prepare sample size calculations for Outline Protocols.
Prepare statistical section for Clinical Study Protocols.
Generate the randomization schedules for clinical trials in accordance with the protocols and maintaining security of schedules before and during the studies.
Provide input to the design of Case Report Forms and review Edit Check Specifications.
Preparation of Statistical Analysis Plans.
Interact with statistical programmers regarding programming requirements for analysis and reporting.
Perform statistical analysis and produce derived datasets for statistical output.
Validation/QC of other statisticians’ analysis.
Prepare the statistical section of top line and Final Clinical Study Reports.
Review Clinical Protocols and Final Study Reports.
Senior SAS Programmer
Working as Senior SAS Programmer, your responsibilities will primarily be as follows:
Provide statistical programming support for assigned project
Review protocols, CRF's, statistical analysis plans, and data submission plans
Develop general SAS application code.
Prepare the data package for a regulatory submissions
Validate SAS programs and analysis results
Import and export data files.
Assists in Quality Control activities
Generate and maintain documentation.
Attends project meetings and departmental meetings
To be eligible for consideration for either position you will have proven experience in the CRO/Pharmaceutical industry, working within the field of clinical trials. You will be educated to a minimum of BSc level for the Senior SAS Programmer position, or MSc for the Senior Statistician role and be able to demonstrate technical competency within the statistical field.
Please apply by CV to [log in to unmask] or telephone +44 (0) 1895 451 806 for a discussion.
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