Dear Allstat,
JOB: Neurology / Oncology / Dermatology Contract Biostatisticians -
Switzerland
Please find below details of the latest SEC Biostatistics opportunity. for
further information contact Alan Brophy on 00 44 (0) 207 255 66 00 or email
[log in to unmask] <mailto:[log in to unmask]>
An opportunity has opened for experienced Biostatistical professionals to
live and work in the beautiful Swiss city of Geneva. The assignments will be
on site with a highly regarded international pharmaceutical organisation for
an initial period of 6 months, with strong possibility of extension.
With this client contractors are not only hired to execute work given to
them, they are given responsibility and are fully integrated in the team of
permanent employees. This is an exciting and challenging position within a
friendly and international environment.
The Role:
The assignments will focus within either Neurology, Oncology or Dermatology
indications. In this role you will:
- Provide statistical input into Phase II, III and IV clinical trial
development.
- Analyse clinical trial data, and statistical input into the reporting of
clinical trial results.
- Provide statistical input into protocol/CRF development in the therapeutic
area of the client (e.g., trial design, sample size estimation,
randomization, statistical methods for protocols, query checks for clinical
trial data).
- Write detailed statistical analysis plans for clinical trials as well as
for integrated summaries of efficacy and safety.
- Analyse clinical trial data producing accurate results representing the
outcome of the trial.
- Validate statistical output.
- Accurately interpret and clearly communicate statistical results and
concepts to non-statisticians.
- Co-author final integrated reports of clinical trial data writing thorough
and clear statistical methods sections and producing the statistical
appendix for the reports are accurately interpreted in the publications.
- Provide input into statistical SOPs and general standardization efforts
within the department (e.g. statistical methodology standards, standard data
presentations).
- Participate in interactions with regulatory agencies as required.
- Collaborate effectively with members of clinical trial implementation
teams and with biometric colleagues.
To secure this assignment you will have a PhD qualification in
Statistics/Biostatistics with 2+ years pharmaceutical / CRO experience or an
MSc Statistics / Biostatistics with 5+ years pharmaceutical CRO experience.
Experience in the specified therapy areas is highly advantageous, Strong SAS
skills are important. Good team working and communication skills are
essential.
Rates of pay will be excellent, full assistance with working visas' and
accommodation/relocation will be provided. Take this opportunity to work and
live in a beautiful Swiss City and gain experience with a leading
pharmaceutical organisation.
For a full discussion of this post call 00 44 (0) 207 255 66 00 or email
[log in to unmask] <mailto:[log in to unmask]>
Kind regards,
Alan Brophy
SEC Recruitment, London
Tel: 0207 255 66 00
Fax: 0207 255 66 01
<mailto:[log in to unmask]> [log in to unmask]
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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