Dear Allstat,
Please find below our latest permanent Statistician role based in the South
East. Ideally our clients are looking for candidates with Oncology
experience but will also consider those without.
If this role is of interest to you please send an update CV to
[log in to unmask] or alternatively for a consultation you can
reach me on +44 (0)207 922 7126
JOB DESCRIPTION
Our clients based near London are actively looking for a well rounded
statistician with good knowledge of SAS and DM. An excellent company which
is currently growing and working in the Oncology Ta.
RESPONSIBILITIES
A Senior Biometrician is required by a leading company to perform a wide
variety of responsibilities within a SAS programming, statistical and data
management environment.
Reporting to the Head of Biometrics, the successful candidate will work
across a wide variety of development programmes.
The ideal candidate will be either a Statistician or a Project Data Manager
with significant knowledge in other areas of biometrics (Data Management,
SAS programming and Statistics), and preferably with CRO management
experience.
An exciting role for an individual looking to have autonomy, a high level of
responsibility and develop project management skills across all areas in
biometrics. The company is a ambitious biotechnology company specialising in
oncology with several drugs in development in Phase I to III.
PRIMARY DUTIES
Manage outsourced biometrics activities such as ongoing data reviews, trial
progress, database lock and reporting of clinical studies
Ensure data standards are adhered to, and involve in the development of new
standards in biometrics
Provide data management and statistics input into trial set-up activities,
and be responsible for the creation of statistical analysis plans, the
specification and programming of datasets and outputs, review of data and
outputs from CROs, and reporting for individual clinical studies
Manage and perform additional analyses for regulatory requests, publications
and other communications
QUALIFICATIONS
For someone from a statistical background, the candidate would ideally be
educated to MSc or higher level in a statistics discipline, with strong SAS
programming skills and good understanding of data management.
For someone from a data management background, the candidate would possess
strong SAS programming skills, numeracy skills and have a good understanding
in statistical reporting of clinical trials.
The ideal candidate should also possess good project management skills and
has experience in CRO management. You will need to demonstrate excellent
written and verbal communication, as well as organisational, interpersonal
and problem-solving skills.
Experience in the set-up and maintenance of data and programming standards,
knowledge of CDISC, CRO management and therapeutic knowledge in oncology
would be advantageous.
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