Hello Allstat

SRG have been recruiting within the clinical trials industry since 1991.
Each of our consultants has worked in the industry, so we understand the
roles that we advertise. We can provide support and advice on living and
working in Switzerland so if you have any questions do not hesitate to
call.
SRG currently have the following Biostatistics and Programming vacancies
and more:

* Biostatistics Therapeutic Area Group Head
Switzerland
Permanent
Excellent salary + package + relocation

An exciting opportunity for an operational manager to head up the
biostats team for this blue chip pharma. You will manage resource,
quality, timelines and efficiency.
You will maintain high scientific standards, ensure deliverables comply
with global regulatory guidelines and act as site head for the Biostats
group to establish and maintain sound working relationships with
partners and customers.
Significant experience working within the pharmaceutical industry and a
PhD is preferable although not essential. You will have worked as a
project statistician for international clinical teams and have excellent
written and spoken English. You must be eligible to work in the EU.
Full role spec available on application.
_______________________________________________________

* Global Statistical Reporting Group Head
Switzerland 
Permanent
Excellent salary + package + relocation

Working alongside the Biostatistics Group Head, your objective is to
contribute and develop the long-term goals and operating policies for
statistical reporting across the organisation. You will initiate and
support continuous improvement initiatives and contribute to the
development of the clinical information systems across the company.
As well as leading the strategic direction of the group you will
recruit, coach, develop and manage direct reports with a view to sharing
these resources across therapeutic areas.
Significant experience within global drug development together with a
PhD or college degree in Life Science, Statistics, Mathematics or
Computer Science is required. A proven track record in successful
project management and line management is a must. You must be eligible
to work in the EU.
Full role spec available on application.
________________________________________________________

* Expert Statistician for Quantitative Safety
Switzerland
Permanent
Excellent salary + package + relocation

This company's clinical pipeline has consistently been ranked by experts
as one of the strongest in the industry. They are seeking a statistical
expert to provide advice to clinical teams for safety related questions
across all phases of development. You will input into the overall safety
strategy, develop risk management and analysis plans for clinical trial
data both at the study and project level.
Masters Degree in Statistics (or equivalent) with significant experience
in clinical trials and, ideally, regulatory submission experience. In
return they will offer you an extremely competitive salary and benefits
package and a working environment that is second to none.
You must be eligible to work in the EU.
________________________________________________________

* Contract Statistical Programmer x 3
Switzerland (Full relocation support provided)
95-110CHF per hour
6-12 month contracts

My client is seeking a number of experienced SAS Programmers to ensure
analysis and data reporting code meet regulatory and company standards.
You will develop programs to support safety and efficacy analysis across
all phases of the drug development process. An experienced
Statistical/SAS Programmer, you will have solid skills in SAS/STAT,
SAS/BASE, SAS Macro and SAS Graph with some pharmaceutical industry
experience.
You must be eligible work in the EU.
_______________________________________________________

Principal Statistician
Switzerland
Permanent
up to 130,000CHF pa + benefits + relocation

Working at this company's headquarters you may manage (dependent on
workload)  a small number of Biostatisticians and/or statistical
programmers focused on a Therapeutic area. You will provide statistical
input for statistically complex protocol development and with limited
direction, write statistical analysis plans & perform statistical
analyse for statistically complex clinical trials. You will also
independently provide statistical input for statistically routine
protocol development and write statistical analysis plans and perform
statistical analysis for statistically routine clinical trials. 
PhD or MSc in related field, extensive knowledge of routine statistical
methodology, proficient in SAS statistical procedures and knowledge of
statistical and clinical regulatory guidelines.
________________________________________________________

* Statistician (Graduate)
Switzerland
Permanent
Salary dependent on experience

Therapeutic area Statistician responsible for all statistical aspects of
individual clinical trials. This opportunity would suit a PhD graduate
statistician with little or no experience within clinical trials as full
training and support is provided. Once trained, you will be responsible
for all statistical tasks e.g. clinical trial design/planning, analysis
plan, reporting activities, exploratory analyses and additional analyses
to support publications and statistical consultation during the running
phase.
At least a Masters in Statistics and 2 years relevant work experience or
if you a posses a PhD. no specific previous job experience required.
You must be eligible work in the EU.
________________________________________________________

Senior/ Statistical Programmer
Switzerland
Permanent
Excellent Salary + package + relocation

You will support statisticians, senior programmers and Group Head by
programming analysis datasets, pooled datasets, listings and tables for
the presentation/reporting of clinical data for Phase I-IV. You will
have access to a large international team of programmers in our Global
Statistical Reporting (SR) group. As a team member, you will interact
with different line functions such as Clinical, Data management,
Biostatistics, Marketing or Drug Regulatory Affairs. 
Minimum of a BA/BS or equivalent experience in mathematics, statistics,
computer science or life science or related field(s), Fluent English
(oral and written) and working knowledge of/ experience with SAS
software. You must be eligible to work in the EU.

For more information or a confidential discussion please call Helena on
+44207 562 1792 or email [log in to unmask]
We have several opportunities so if you want to talk through your
options of working overseas I am happy to help.




Helena Newman-Mitchell
Consultant

T: +44 (0)20 7562 1792
F: +44 (0)20 7562 1799
M:+44 (0)78 2536 2548
E: [log in to unmask]
W: www.srginteresource.com

I work Monday- Thursday 



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