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ALLSTAT  August 2008

ALLSTAT August 2008

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Subject:

Fantastic opportunity for Contract Biostatistician with major Pharma in Switzerland

From:

Fforde Management <[log in to unmask]>

Reply-To:

Fforde Management <[log in to unmask]>

Date:

Tue, 19 Aug 2008 10:11:17 +0100

Content-Type:

text/plain

Parts/Attachments:

Parts/Attachments

text/plain (70 lines)

Biostatistician (Contract)
Ref: 14082

This is an excellent opportunity for a Biostatistician, with some relevant 
statistical experience from working in clinical trials in the biopharmaceutical 
industry, to work for one of the established pharmaceutical world leaders at 
their office in Switzerland.  This is a contract role for 12 months which may be 
extendable and the company is providing a free, furnished apartment.

JOB ROLE – Principal Responsibilities:   
With direction performing the following activities:
•	Providing statistical input for statistically routine protocol and CRF 
development and query checks.
•	Writing analysis plans for statistically routine clinical trials including 
the most appropriate statistical methodology and data presentations. 
•	Providing statistical analysis for routine clinical trials.
•	Writing accurate, thorough and objective statistical methods 
sections for statistically routine integrated final reports. 
•	Reviewing statistically routine integrated draft reports ensuring 
the accuracy of the statistics.  
•	Regulatory Submissions/Contacts – applying, as appropriate, ICH 
statistical and clinical report guidelines.
•	Performing routine statistical analysis for manuscripts.
•	Programming and validating tables and derived listings as required.
•	Understanding and following all statistical and statistical 
programming SOPs.
•	Providing leadership to non-statistical colleagues with routine 
statistical issues.
•	Participating effectively on teams for statistically routine clinical 
trials. 
•	Producing assigned work within the timelines provided ensuring 
deadlines are met.
•	Keeping abreast of statistical developments.

QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
•	PhD or MSc with relevant experience in the 
pharmaceutical/biotech industry.
•	Fundamental knowledge of, and with direction, application of 
routine statistical methodology.
•	Clinical knowledge including the ability to develop a familiarisation 
within relevant clinical areas.
•	Working knowledge of SAS and proficient in SAS statistical 
procedures.

PERSONAL SKILLS & ATTRIBUTES
•	Excellent communication skills. 
•	Good problem solving skills.
•	Team Working

BENEFITS OF THE ROLE: This solid, well established company aims to develop 
and retain the best talent in the industry by maintaining a proactive and 
creative work environment where individuals can actively contribute to the 
company’s success.  They are offering a competitive remuneration which may 
be taken as a salary or on a daily rate and a fully furnished apartment in 
Switzerland plus one flight per quarter paid.  

Fforde is a uniquely specialised recruitment agency/business for the 
pharmaceutical, clinical research and biotechnology sectors.  For applications 
please email your CV to: [log in to unmask] or speak to our 
specialist consultant, Aura Rico on +44 (0)20 3008 4421 who will be pleased 
to give you further information and advice on your personal career needs.  
Visit our website and see all our job opportunities at www.fforde-
management.com


KEY WORDS:  Biostatistician, Statistician, Biostatistics, Statistics, Clinical 
Trials, Protocol Development, CRF Development, Statistical Methodology, 
Regulatory Submissions, Statistical Analysis, Statistical Reporting, Statistical 
Programming, Validating, SOPs, PhD, MSc, SAS

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