LISTSERV at the University of Georgia
Menubar Imagemap
Home Browse Manage Request Manuals Register
Previous messageNext messagePrevious in topicNext in topicPrevious by same authorNext by same authorPrevious page (April 2004, week 3)Back to main SAS-L pageJoin or leave SAS-L (or change settings)ReplyPost a new messageSearchProportional fontNon-proportional font
Date:         Tue, 20 Apr 2004 11:35:32 -0400
Reply-To:     Natalie Fforde <natalie@FFORDE-MANAGEMENT.COM>
Sender:       "SAS(r) Discussion" <SAS-L@LISTSERV.UGA.EDU>
From:         Natalie Fforde <natalie@FFORDE-MANAGEMENT.COM>
Subject:      Statistical Consultant : expert to support early Clinical
              developement , based in Switzerland or USA
Content-Type: text/plain; charset=ISO-8859-1

As a senior member of the ECD Biostatistics group, you will oversee a range of projects in one or more disease areas. You will • work closely with a team of experts from Research, Development, Regulatory Affairs and Marketing to provide statistical expertise for early Clinical Development Plans, • contribute to strategic discussions and decisions on the project level, • represent Biostatistics in the early International Clinical Team, • and work with other statisticians to give guidance and expertise on the design, analysis and reporting of clinical trials.

You continuously strive for innovative solutions for our projects and studies, and you will develop and implement novel statistical procedures in design or analysis. You will work with our Modeling and Simulation group to explore data for product profiling, hypothesis generation, new research topics and publications. For this you will have access to an international team of internal and external statistical methodology consultants. In addition, you will interact with health authorities, external experts and opinion leaders to support and defend project plans and data analyses and their interpretation. You will also oversee the preparation of regulatory documents, like INDs.

Your qualifications: • University degree in Statistics or Mathematics (Ph.D. or MSc. level) • At least seven years relevant experience in the field of clinical trials (for Ph.D. 4 years) are a must • Good knowledge of clinical trials methodology and proven knowledge of drug development process and Health Authority guidelines and regulations • Basic knowledge of pharmacological/physiological sciences and PK/PD would be a plus • Good knowledge of scientific computation and SAS, S-Plus are an advantage. • Flexible, positive, creative thinker, good communicator, negotiator and team player • Good leadership skills and project management skills are required.

Natalie Fforde Managing Director Fforde Curtis House 34 Third Ave Hove BN3 2PD

Tel: 01273 722366 Fax: 01273 325350 Mobile: 07769 700 222 Email: natalie@fforde-management.com


Back to: Top of message | Previous page | Main SAS-L page