CONTRACT: Statistical Programmer
UK Based
6 -12 month Contract Position
Job Summary:
Working for a very well respected pharmaceutical company, in the European offices of their global Operations. This position provides SAS programming expertise to the analysis of Phase II, III and IV clinical trial development.
Accountabilities/Responsibilities:
* Provide input into CRF & query specifications to collect and clean data specified in the protocol
* Provide input into analysis plan and data presentations for clinical trials.
* Program (or write validation programs for) and document derived datasets, tables, derived listings and/or graphs for clinical trials or portions of clinical trials
* Mentor biostatisticians and statistical programmers in more advanced SAS programming techniques.
* Perform the lead programmer role on trials, as required, this involves working with the statistical programming manager to prepare forecasts and timelines, represent the function in trial team meetings and co-ordinate the work of programmers to deliver results on time.
* Contribute to the writing or review of statistical programming SOPs as required.
* Provide input into general standardization efforts (e.g., CRF's, query checks, standard statistical programs, data presentations).
* Create and validate global macros that streamline repetitive and critical operations and increase programming efficiency.
* Provide statistical programming for regulatory reporting and submission processes (eg. E-submissions)
* Communicate technical programming concepts to statistical programmer/analysts and biostatisticians in a clear, concise, focused and articulate manner
Essential Skills & Capabilities:
* MSc or BSc in Statistics or equivalent
* 3-5 yrs pharmaceutical or biotech / any other relevant experience
* Expertise SAS/BASE, SAS/STAT
* Knowledge of SAS/CONNECT, SAS/MACRO, SQL
* Ability to solve complex problems logically
* Interpersonal skills, initiative, creativity.
* Excellent communication skills.
An excellent opportunity awaits for this renewable contract. Interview times booked and full job specification to review...
If you would to discuss this role in greater detail or your application / suitability to this or further roles, please call me or email me in confidence. If you are not available or suited to this position, please feel free to pass my details on.
We also have a broad variety of other Biometric specific vacancies available in the UK and throughout Europe. Inclusive of SAS programming, Statistical, Clinical programming, Data Management functions, Regulatory Affairs, Clinical Research, QA, Compliance & Validation.
For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV to [log in to unmask]
James Carrera
Manager - Pharmaceutical, Healthcare & CRO Division
Tel: +44 (0) 207 255 6665 [log in to unmask]
Fax: +44 (0) 207 255 6656
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