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Dear Allstat

Our pharmaceutical industry client, with offices in the South East of England, Germany and France, are looking to recruit a permanent project statistician.  It would be possible to work from any of these locations. The rate is up to £50 p/h dependent upon experience. 

You will develop or assist in the development of protocol designs, clinical plans, and data analysis plans in collaboration with physicians, veterinarians, and/or medical colleagues. The Project Statistician is responsible for working with research associates and scientists to establish a reporting database and for analyzing data for these types of studies. 

* Operate in collaboration with study personnel to provide input on study protocol, design studies and write protocols for the conduct of each study. 
* Assist in or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol, and conducting the actual analysis once a reporting database is created. 
* Collaborate with data management in the planning and implementation of data quality assurance plans. 
* Maintain currency with respect to statistical methodology, to maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected. 
* Participate in peer-review work products from other statistical colleagues. 
Communication of Results and Inferences 
* Collaborate with team members to write reports and communicate results. 
* Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings. 
* Respond to regulatory queries and to interact with regulators. 

Therapeutic Area Knowledge 
* Understand disease states in order to enhance the level of customer focus and collaboration and be seen as a strong scientific contributor. The specific area will be late phase Oncology.

Regulatory Compliance 
* Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Ccorporate, Mmedical, local, and departmental policies, procedures, processes, and training.

OTHER INFORMATION 

* Proficiency in the SAS programming language 
* Interpersonal communication skills for effective customer consultation and presentations 
* Teamwork and leadership skills 
* Resource management skills 
* Demonstrated problem solving ability and strategic thinking 
* Business process expertise associated with critical activities (e.g. regulatory submissions) 

Education required: M.S., Ph.D., or equivalent experience in a Statistics, Biostatistics, or equivalent discipline


If you are interested in this vacancy then please contact Tim Barratt at Key People on: 

[log in to unmask]  or by telephone on +44(0)1727 817 626

You can see our other vacancies at www.keypeople.co.uk 

Kind regards

Tim Barratt
Recruitment Resourcer
Key People Ltd
Catherine House, Adelaide St, St Albans, Herts, AL3 5BA
Direct Tel: 01727 817 626 / Office: 01727 811634 / Fax: 01727 844838
E-Mail: [log in to unmask] / Web Page: http://www.keypeople.co.uk/
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