Principal Statistical Programmer

Employer
Covance
Location
Rueil-Malmaison, , France
Salary
Competitive
Closing date
4 Oct 2020

View more

Discipline
Data Management / Statistics, Statistical Programming
Hours
Full Time
Contract Type
Permanent
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Job Overview:
  • Principal Statistical Programmer required to work for Covance
  • You will be employed by Covance working in our late phase (II-IV) full-service group with the opportunity to work across several therapeutic areas
  • Home based anywhere in Europe or South Africa
  • You must have previous experience of working as a Lead Statistical Programmer in either a biotech, CRO or pharma company using the SAS programming language
  • Candidates must be fluent in English language (both verbal and written)

Join our growing team and discover your extraordinary potential by working as a Covance Principal Statistical Programmer. As a Principal Statistical Programmer at Covance you will be responsible for all statistical programming deliverables of one or more complex clinical trials. You will work in our internal late phase full service group so you will enjoy a varied role working for different sponsors across several therapeutic areas within phases II-IV. The position offers a strong support network, flexible working solutions and the opportunity to progress your career. If you are an experienced Lead Statistical Programmer and you are looking for your next career move then this is a fantastic opportunity. This really is an incredibly exciting time to be joining Covance as we continue to grow and expand. This is a permanent, full-time office or home-based role anywhere within Europe or South Africa.

Job Primary Functions
  • Perform the role of the Lead Statistical Programmer.
    • Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments and the client, etc.
  • Develop and maintain SAS programs to create complete SDTM and ADaM datasets and TFLs, and perform QC of SDTM, ADaMs and TFLs
  • Produce Define XML/PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs
  • Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets and contribute to the development of Covance and Client standards
  • Review SAPs and TFL shells from a programming perspective for studies and advise on the development of complex TFL shells from a programming perspective
  • Mentor less-experience programmers in the processes around SDTMs, ADaMs and TFLs ensuring adherence to department practices and processes
  • Present and share knowledge at department meetings
  • Respond to QA and client audits and support qualification audits
  • Contribute to proposal activities and participate in bid defenses meetings in order to win new business
  • Continually identify and suggest ways to improve the efficiency, quality and productivity of statistical programming
Education/Qualifications:
  • BSc, preferably in computing, life science, mathematical or statistical subject
Experience:
  • You must have previous experience of working as a Lead S tatistical Programmer on complex studies in either a biotech, CRO or pharma company using SAS
  • Knowledge in all aspects of clinical trials from initial study set-up to study completion with an excellent understanding of the roles and responsibilities of all related disciplines, e.g. Biostatistics and Clinical Data Management.
  • Broad knowledge of all CDISC requirements related to SDTM and ADaM, including define.xml, Reviewer's Guide and submission standards
  • Excellent organizational, time management and project management skills with team leadership experience, as demonstrated by ability to organize and motivate project teams and the ability to delegate and prioritize work to meet project timelines
  • Self motivation and ability to work independently without appreciable direction
  • Ability to apply extensive technical expertise and the full knowledge of other related disciplines to provide consultancy and advice on programming and wider related issues to other departments and disciplines
  • Excellent problem solving skills, a proactive approach, anticipating issues and working to ensure they are avoided or resolved as quickly as possible
  • A willingness to make decisions seeking advice from statistical programming managers or directors to confirm decisions when necessary
  • A proactive approach to developing and maintaining effective working relationships with staff in other disciplines, often in other locations and in working to achieve consistent processes and standards across them
  • Candidates must be fluent in English language (both verbal and written)


PLEASE NOTE CANDIDATES WHO DO NOT FULFIL THE CRITERIA MAY NOT RECEIVE A RESPONSE

NO AGENCIES PLEASE

MORE INFORMATION AVAILABLE ON REQUEST

For a confidential discussion about this opportunity, please phone Peter Lewis on +44 (0) 1628 543 457 . To apply, please click on the APPLY button.

Keywords:

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Join our growing team and discover your extraordinary potential


We are recognized as a leader in drug development because of our exceptional people. At Covance, we embrace and celebrate the different strengths, experiences and perspectives of our 20,000+ team members across the globe. Our team is driven by an energizing purpose to improve health and improve lives. Here, you can play a role in bringing new scientific discoveries to life and make a difference in the lives of millions. And, our comprehensive service portfolio provides the opportunity to explore diverse projects and unique career paths across the drug development spectrum.

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Learn more about our work to improve health and improve lives:

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Contact Us
  • Maidenhead Office Park
  • Westacott Way
  • Maidenhead
  • SL6 3QH
  • United Kingdom
  • Mini-site: Covance
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