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ALLSTAT  August 2008

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Subject:

Contract Biostatistician for RTP, North Carolina

From:

Fforde Management <[log in to unmask]>

Reply-To:

Fforde Management <[log in to unmask]>

Date:

Mon, 18 Aug 2008 15:25:24 +0100

Content-Type:

text/plain

Parts/Attachments:

Parts/Attachments

text/plain (61 lines)

Biostatistician (Contract)
Ref: 00383

This is an excellent opportunity for an experienced Biostatistician to work for a 
unique CRO that specializes in studies only using EDC.  They manage Phase I-
IV clinical trials combining advanced technology with expert clinical knowledge 
and experience in a wide variety of therapeutic areas.  This is a contract 
position for 12 months based at the company’s office in RTP North Carolina. 

JOB ROLE:  The Biostatistician will provide statistical consulting and technical 
support related to the design and statistical analysis of clinical studies.  This 
includes:
•	Providing statistical consultation for clinical programs
•	Participating in eCRFs design and the corresponding edit checks
•	Determining the analysis and data presentation specifications for 
programmer analysts.
•	Performing statistical analyses.
•	Interpreting study results.
•	Collaborating with medical and biostatistics staff to produce 
interim reports and final reports.
•	Ensuring that the biostatistics portions of project timelines are 
met with superior quality deliverables.

QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
•	BS in Life Sciences and 7 years related experience.
•	Or MS in Mathematics or Biostatistics with 4 years related 
experience.
•	Or doctorate-level degree in Statistics or Biostatistics with 1 year 
related experience.  
•	Data handling or analysis experience required.
•	Knowledge of the biostatistical, programming, and data 
management aspects of the clinical research service industry.
•	Understanding of GCP, ICH, and FDA guidelines and regulations 
applicable to conduct clinical research.
•	Experience with the management and statistical analysis of data 
obtained from Phase I - IV clinical trials.
•	The ability to synthesize results in graphic, oral, and written 
reports.
•	Experience using SAS (including data manipulation) and other 
software packages such as SPSS, S-Plus.

PERSONAL SKILLS & ATTRIBUTES:
•	Excellent interpersonal and organization skills, highly detail-
oriented.  
•	Good oral & written communication skills.
•	Willingness to learn new programming languages, new technology, 
and new tools.

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, Damon Bacote on +1 212 520 8304 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, Biostatistics, Statistician, Clinical Statistician, 
Statistics, Statistical Analysis, Statistical Design, Statistical Reporting, Clinical 
Studies, Clinical Trials, Phase I-IV, Protocols, eCRF Design, CDF Specifications, 
SAS Programming, SPSS, S-Plus, Life Sciences, Mathematics, BS, MS, 
Doctorate, Data Analysis, GCP, ICH, FDA

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