Hi All.
 
SRG Clinical currently have a vacancy with one of the world leaders of
the pharmaceutical industry for a Senior Statistician on a permanent
basis to support their oncology drug development portfolio.  With
offices based all over the world you would be situated at one of the key
sites in the South East.  The company has been a pioneer in the
healthcare industry for over 80 years and they have a mission to add
continuous value to the pharmaceutical industry through its expertise,
focus and tailored approach. 

 

As a senior statistician you will be responsible for both the
statistical analysis and project management of various clinical project
across phases 2 and 3 of the oncology therapeutic area.  The senior
statistician will be involved in the preparation of drug development and
statistical analysis plans to ensure all statistical methods, output
deliveries and timescales are achievable and can be delivered
efficiently.  You will develop strategies for clinical development plans
and will be able to input ideas into the development of new standards
policies and procedures.  As the senior statistician you will act as a
key figure within the team and will be responsible for maintaining a
high quality of work to current regulations and guidelines including ICH
and GCP, notifying senior managers of any issues, deviations or delays
in the output.  You will also perform resource planning and will
organize workloads to ensure timely delivery.  In addition, as the
senior statistician there will be an element of programming statistical
outputs and validations using SAS.

 

A successful candidate will have

 

*	A minimum of an MSc, or equivalent, in a relative degree subject
*	A strong background working within industry in a pharmaceutical
company or Contract Research Organisation (CRO)
*	Experience of statistical analysis such as tables, listings,
figures along with validations and the production of statistical
analysis plans
*	Familiar with current standards and regulations including GCP
and ICH
*	Project Management experience and ability to lead a study team
*	Knowledge of statistical software in particular SAS is necessary
*	Excellent communication skills at all levels
*	Ability to establish and maintain good working relationships
with the ability to present ideas and contribute to professional
meetings and training programs.

This is a great opportunity for you to join a leading pharmaceutical
company and be able to develop your project management skills as a
statistician within the clinical trials industry.

 

Please get in touch for more information.  We also offer a great 'refer
a friend' scheme so if you have any colleagues or friends who will be
interested in the above please feel free to pass across my details.

 

Many thanks for your time,

 

Rhianne

 


Rhianne Tsai BSc (Hons) MIRP CertRP
Account Executive	
Direct Tel:  +44 (0) 207 562 1790
Fax:           +44 (0) 207 562 1799
Mobile:      +44 (0) 7787 102 629
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