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Job Details

Senior Statistical Programmer (SAS)

Company: Chiltern
Location: Office based in Toulouse, France or homebased anywhere in France
Reference: PL-900222-FR
Closing Date: 16 Nov 17
Type: Full Time
Salary (£): On Application
Benefits: Excellent and competitive benefits

Job Summary:

• Senior Statistical Programmer (SAS) required to work Chiltern. You will be seconded to work 100% dedicated to a pharmaceutical client. • Office based role, Toulouse, France or Home Based anywhere within France. • The Senior Statistical Programmer must have a minimum of 4 years’ experience working within a Pharma/Biotech or CRO and have CDISC experience. • The Senior Statistical Programmer must be able to start work during November 2017 at the latest

Requirements:

Job Background

  • Senior Statistical Programmer (SAS) required to work Chiltern.  You will be seconded to work 100% dedicated to a pharmaceutical client.
  • Office based role, Toulouse, France or Home Based anywhere within France.
  • The Senior Statistical Programmer must have a minimum of 4 years’ experience working within a Pharma/Biotech or CRO and have CDISC experience.
  • The Senior Statistical Programmer must be able to start work during November 2017 at the latest
  • The Senior Statistical Programmer must have the legal authorisation to work in France

 

Description

Chiltern is seeking top talent for positions within our Source division which is a unique and well established business unit within Chilterns’ Strategic Staffing Provision.  They employ and second clinical research professionals to biotechnology and pharmaceutical companies globally.  In this role the Statistical Programmer provides statistical software and software documentation support to biometrics in general and to specific clinical projects. He/She takes responsibility for the planning, development, validation, documentation and maintenance of SAS code to support project work.

 

Job Primary Functions

  • Perform data manipulation techniques and advanced techniques (arrays, transpositions, complex merges, SQL, etc.) and generic macro use and development to enable listing, table and graph generation
  • Analyze information and develop innovative solutions to programming and data analysis challenges
  • Efficiently produce quality results under time constraints
  • Successfully coordinate multiple priorities
  • Complete assigned tasks within known budget constraints
  • Serve as the statistical programming lead on internal project teams and coordinate programming, verification, and documentation of statistical programs for use in creating analysis datasets, tables, listings, and figures
  • Assist internal project team in identifying project priorities and communicating such activities and associated timelines to departmental management
  • Work independently to carry out assignments with occasional support from senior management
  • Ensure the efficiency, quality, and integrity of data reporting and project activities executed
  • Represent the department in client meetings/presentation and maintain a positive working relationship with sponsors, collaborating associate and vendor personnel
  • Actively adapt and adjust priorities to ensure timely and quality completion of assigned tasks
  • Contribute to ongoing improvement of programming processes and methodology
  • Perform other related duties as required by the Department.

 

Job Qualifications

  • Undergraduate degree or higher in Biostatistics, Computer Science, or related field
  • Minimum 4 + years of experience, or an equivalent combination of education or experience to successfully perform the key responsibilities of the job
  • Must have CDISC experience
  • Previous experience in a pharmaceutical research or CRO setting required
  • Knowledge of one or more statistical software packages (SAS® preferred) used to conduct statistical analyses
  • Good verbal and written communication
  • Fluent in English language (both verbal and written)
  • Candidates must have the legal authorisation to work in France

 

MORE INFORMATION AVAILABLE ON REQUEST

For a confidential discussion about this opportunity, please phone Peter Lewis on +44 (0) 1753 216 727.  To apply, please send your CV to peter.lewis@chiltern.com - peter.lewis@chiltern.com

 

About Chiltern:

Chiltern, a global contract research organization, is a leading provider of clinical services and solutions in a variety of therapeutic areas with engagement models for biopharmaceutical and medical device industries. Chiltern’s team of more than 4,300, located across 47 countries, provides comprehensive Clinical Development, Medical & Scientific Affairs, Data & Analysis, Pharmacovigilance and Strategic Regulatory services using a collaborative approach for more efficient clinical trials. Visit Chiltern.com to learn more about how Chiltern is Designed Around You®.

 

Keywords:

Programmer Analyst, Stats Programmer, Senior, Statistical Programmer, Lead, SAS Programmer, CDISC, ADaM, SDTM, Biostatistics, Senior Statistician, Statistician, Biostatistician, Stato, Statistics, Study Biostatistician, pharma, pharmaceutical, France, SAS, STAT, home based, SAS, Toulouse, pharma, pharmaceutical, home-based, field based, flexible working, flexible location.



Chiltern is an EEO / AA Employer and is committed to providing opportunities to minorities, women, individuals with disabilities and veterans.

Salary

on application

Position Type

Permanent or Contract
Full Time

Contact

Email Peter Lewis - Peter.Lewis@chiltern.com
+44 (0) 1753 216 727

Apply for this job: Senior Statistical Programmer (SAS)

Contact Information:

Address:  London, UK
171 Bath Road Slough Berkshire
SL1 4AA, UK
England
Tel:  +44 (0) 1753 512000
Fax:  +44 (0) 1753 511116
Website:  Visit Our Web Site

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