Senior Statistician/Biostatistician - Surrey
Freelance 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:
- Providing scientific statistical input to development plans and to project planning.
- Providing representation on project teams
- Providing statistical consultancy to other departments on request.
- Making study design recommendations and preparing sample size calculations for Outline Protocols.
- Preparing statistical section for Clinical Study Protocols.
- Generating the randomization schedules for clinical trials in accordance with the protocols and maintaining security of schedules before and during the studies.
- Providing input to the design of Case Report Forms and review Edit Check Specifications.
- Preparing of Statistical Analysis Plans.
- Interacting with statistical programmers regarding programming requirements for analysis and reporting.
- Performing statistical analysis and produce derived datasets for statistical output.
- Validating/QC of other statisticians’ analysis.
- Preparing the statistical section of top line and Final Clinical Study Reports.
- Presenting and discussing results with internal/external bodies as required.
- Reviewing Clinical Protocols and Final Study Reports.
- Approving Case Report Forms.
- Working 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 position is full time and office based in Surrey, 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.
If you have the required experience for any of the advertised roles and would like to apply for them, then please apply by CV to [log in to unmask] or telephone +44 (0)1895 451 806 for a discussion.
If the above opportunity is not suitable, but you would be interested in other opportunities then please send your CV with details of the types of position you are looking for.
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