Senior Statistician/Biostatistician - Surrey & Middlesex (Contract/Permanent)
inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies, offering therapeutically specialized capabilities for Phase I-IV clinical development, bioanalytical services, and strategic resourcing from a single clinical professional to an entire functional team. With 7,000 passionate employees in more than 36 countries, inVentiv Health Clinical works to accelerate high quality drug development programs of all sizes around the world.
inVentiv Health Clinical is currently recruiting for experienced Statisticians for a number of positions as Senior Statistician, working on clinical trials.
Working through our Strategic Resourcing Staffing division, the position is working at our client site, a leading Pharmaceutical and Consumer Health company and is an excellent opportunity for someone with Statistical experience within clinical trials to work both at a technical and project level. You will gain broad experience in a growing field of clinical development and working within inVentiv Health Clinical will enable you to have long term future development within a leading provider of global drug development services.
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 Provision of statistical consultancy to other departments on request.
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.
Present and discuss results with internal/external bodies as required.
Review Clinical Protocols and Final Study Reports.
Approve Case Report Forms.
Works with inVentiv Health Clinical as needed for project work.
To be eligible for consideration you will have a number of years experience as a Statistician in the CRO/Pharmaceutical industry and a MSc (or higher) degree in a related field of Statistics.
The positions are full time and office based in Surrey and Middlesex, UK and can be offered either as a freelance contract (renewable), or through a contract of employment. Excellent rates of pay or a competitive salary plus benefits are on offer for candidates with the right experience.
Please apply by CV to [log in to unmask] or telephone +44 (0) 1895 451 806 for a discussion.
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