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Covance Principal Statistical Programmer in Leeds, United Kingdom

Job Overview

  • Principal Statistical Programmerrequired to work for Covance

  • Excellent opportunities to progress

  • Varied, fast paced environment

  • Office based in Leeds, Yorkshire, UK or work from home anywhere in EuropeCandidates must haveexperience of working as a Lead Statistical Programmer within a Biotech, CRO or Pharma company within Europe

Join our growing team and discover your extraordinary potential by working as a Covance Principal Statistical Programmer within our Early Phase (Phases I & II) statistical programming department. As a Senior Statistical Programmer at Covance you will provides technical leadership with responsibility for delivering SAS programming services to clients and project teams, whilst maintaining optimal department processes and implementing effective project specific strategies. The Principal Statistical Programmer will work with the senior team to provide guidance, mentoring and training to SAS Programmers to ensure best working practices are maintained.

Working within early phase statistical programming we offer, in a word, variety

In the type of studies: PK, Bioequivalence, Metabolism, Dose Escalation etc. and Sponsors

  • In Early Phase we are not assigned for years to the same study, so you will be exposed to multiple studies for clients with different needs as well as working with talented internal colleagues

Job Primary Functions

  • Act as a Lead Programmer for projects, and act as a Statistical Programming consultant to clients and internal customers

  • Develop and review SAS programs and output as required

  • Review draft and final production runs for projects to ensure quality and consistency

  • Interact with project team members e.g. Clinical Data Management, Biostatistics and Medical WritingProvide technical support in SAS Programming to global clinical pharmacology

  • Represent Global Clinical Pharmacology during system validation and implementation as required; providing input and follow up as appropriate

  • Prepare and conduct technical training to Global Clinical Pharmacology

  • Work proactively to implement process change, working individually or leading a team as appropriate

  • Have input into writing and reviewing CCRU SOPs and associated documents

  • New technology / methods. Reading up and implementing new methods when necessary

  • Maintain accurate records of all development work undertaken, including but not limited to requirement documentation, testing and user and support manual

Education / Qualifications

We're looking for Programmers ideally educated to degree level: especially interested in a computing, mathematical, statistical subject, or Life Science.

Experience

You should be able to demonstrate a robust and comprehensive expertise working as a Lead SAS Programmer in the clinical research industry, either at a Pharma company or a CRO; and an understanding of the fundamental principles of programming, program development and review.

Show evidence of and experience of leading studies and experience in study set-up and review of study specific documents.

You must be fluent in English language (both verbal and written).

If you're looking for a role in a fast-paced environment leading multiple studies for key clients then Covance is the place for you!

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

NO AGENCIES PLEASE

Keywords:

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Job Number 2019-31930

Job Category Biostatistics/Programming

Position Type Full-Time

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.

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