Dear Allstat,
Statistical Programming Contract Opportunities - South East UK
This major Biopharmaceutical organisation requires the expertise of
experienced Statistical Programmers on 9 month extendable contracts. Rates
of pay are highly competitive, start dates will be for May/June. Working
environment is dynamic and there will be an opportunity to work across a
variety of projects in this role.
Experience of ISS/ISE would be desirable as the team in slough will be
concentrating on submission activities.
NATURE & SCOPE
- Provide programming support and validation of analysis data sets, pooled
datasets, statistical summary tables, figures and patient data listings for
phase I - phase III clinical trials, ISS & ISE, primarily using SAS.
- Provide output for the Clinical Study Report, the Integrated Summary of
Safety (ISS), the Integrated Summary of Efficacy (ISE) and electronic
submissions.
- Based in Slough, will work with biostatisticians and programmers based
also in other sites (Atlanta/Braine).
- This position will require a significant training investment for the use
of UCB conventions in SAS macros, creation of analysis data sets and dataset
structures. Need for ensuring standardization of programs where applicable.
- Apply knowledge of clinical data, the design and phases of clinical
trials, statistics, relevant regulations and the pharmaceutical industry to
the implementation of tasks.
- Handle complex statistical programming issues independently and be
familiar with study programming issues. Bring ideas for new projects and
take the initiative to solve issues.
SPECIFIC SKILLS
- SAS expert
- Fluent in English
- Ability to evaluate processes and situations in an orderly and rational
manner asking questions and identifying missing information.
- Must be able to determine relationships between different parts of a
problem and identify appropriate solutions.
- Accurately and efficiently work towards quality results
EXPERIENCE
At least 3-4 years Statistical SAS programming experience with prior
experience in pharmaceutical related field is required.
Working knowledge of clinical legislation (FDA, EMEA), Good Clinical
Practice (GCP) and Clinical Data Interchange Standards Consortium (CDISC) is
a plus.
STARTING DATE & DURATION
Starting date: June-July.
Contract duration: 9 months
If you meet the above requirements forward your current CV in reply with a
short cover note detailing your rate expectation, notice period/availability
and contact details. Alternatively call Alan on 020 7 255 66 00 for full
details.
Kind regards,
Alan
Alan Brophy
SEC Recruitment, London
Tel: 0207 255 66 00
Fax: 0207 255 66 01
alan.brophy@sec <mailto:[log in to unmask]> pharma.com
SEC are an ISO9001:2000 accredited specialist recruitment company working
within the Pharmaceutical, Biotech and CRO industries. If you are interested
to learn more about further appointments within Biostatistics or Statistical
Programming across the UK and Mainland Europe contact Alan on 020 7 255 6600
for a confidential discussion.
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