A number of excellent opportunities have arisen to work for our client, a
large multi-national Pharmaceutical Company based in Surrey. We are looking
for five experienced statisticians from the more junior with at least one
year's experience to more senior with at least five years plus. The
successful candidates will be responsible for providing statistical advice,
analysis and reporting for allocated clinical trials over a wide range of
therapeutic areas including Primary Care, Oncology and Critical Care.

In addition you will be expected to assist in the development of protocol
designs, clinical plans, and data analysis plans in collaboration with
physicians and medical and paramedical colleagues. Also you will be
responsible for working with systems analysts and CRAs to establish a
reporting database and for analyzing clinical trial data for these types of
studies. The level of responsibility in each of these tasks will be
developed in line with the level of your statistical and operational
expertise and experience.

Key responsibilities will include:

Statistical Trial Design and Analysis
Operate in collaboration with product team medical personnel, global health
outcomes personnel, and possibly others to provide input on study protocol,
design studies and write protocols for the conduct of each study. Will
assist in or be accountable for selecting statically methods for data
analysis, authoring the corresponding section of the protocol, and
conducting the actual analysis once a reporting database is created. Will be
expected to collaborate with data management in the planning and
implementation of methodology, to maintain proficiency in applying new and
varied methods, and to be competent on justifying methods selected. May be
required to peer-review work products from other statistical colleagues.

Communication of Results and Inferences
Will collaborate with other product team members to write reports and
communicate results. Will assist or be responsible for communicating study
results via regulatory submissions, manuscripts, or oral presentations in
group settings, as well as for communication one-on-one with key customers
and presenting at scientific and therapeutically-focused meetings. May also
be asked to respond to regulatory queries and to interact with regulators.

Therapeutic Area Knowledge
Become familiar with disease states in order to enhance the level of
customer's focus and collaboration. Ideally, the successful candidate will
be seen as a strong scientific contributor.

Compliance with Policies and Procedures
Will perform work in full compliance with Company Global Policies and
Procedures, and will be responsible for following applicable departmental
and regulatory guidelines as appropriate.

The ideal candidate will have:

* Good knowledge of SAS
* Interpersonal/teamwork and communications skills for effective
customers consultation
* Leadership skills
* Technical growth and application with working knowledge of
experimental design and statistics
* Self-management skills with a focus on results for timely and
accurate completion of competing deliverables

In addition experience of the following would be beneficial:
* Rescue management skills
* Creativity and innovation
* Demonstrated problem solving ability and strategic thinking
* Business process expertise associated with critical activities like
regulatory submission.

You will have at least an M.Sc., Ph.D.., (or equivalent experience) in the
field of Statistics, Biostatistics, or equivalent in addition one year or
more experience in statistical consulting or clinical research is strongly
desired.

In return you will receive an excellent remuneration package and all large
company benefits.

To apply, please send your CV and covering letter to the address below or by
email to [log in to unmask] quoting the reference above.

Ashley Gilroy
Resource Provision Executive