Senior Statistical Programmer (Oncology)

Senior Statistical Programmer (Oncology)

10 Sep
|
Labcorp Drug Development
|
Centurion

10 Sep

Labcorp Drug Development

Centurion

Job Overview:



- Senior Statistical Programmer required to work for Labcorp Drug Development as a Lead Statistical Programmer

- You will be employed by Labcorp Drug Development working in our Clinical Development Services division working across multiple Sponsors in a dedicated team that works purely on Phase I and IIa patient oncology studies

- Home based anywhere in Europe or South Africa

- You must have previous experience of working as a Lead Statistical Programmer within clinical trials using SAS

- Oncology experience desirable but not essential

- Candidates must be fluent in English language (both verbal and written)









Join our growing team and discover your extraordinary potential by working as a Labcorp Drug Development Senior Statistical Programmer within our Global Clinical Development Statistical Programming department. Within this department there is a team that works solely on Phase I and IIa patient oncology studies across multiple Sponsors. The position offers a strong support network, flexible working solutions and the opportunity to progress your career. If you are looking to strengthen your Lead expertise within a varied and dynamic environment, then this is a fantastic opportunity. This is a permanent, full-time office or home-based role anywhere within Europe or South Africa.



Job Primary Functions



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

- 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

- Develop and review SAS programs and output for SDTMs, ADaMs and TFLs, including submission deliverables e.g. Define XML/PDFs, Reviewers Guides, Analysis Results Metadata (ARM).

- 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

- Proactive involvement with process improvements, investigating and implement new procedures / methods when necessary



Education/Qualifications:



- BSc, preferably in computing, life science, mathematical or statistical subject



Experience:



- You must have previous experience of working as a Lead Statistical Programmer on complex studies within clinical trials using SAS

- Oncology experience desirable but not essential

- An understanding of the fundamental principles of programming, program development and review

- Broad knowledge of all CDISC requirements related to SDTM and ADaM, including define.xml,

- Reviewer's Guide and submission standards

- Positive attitude and willingness to learn and contribute in a team setting and communicate effectively within the team environment

- Good organization skills and the ability to prioritize own work

- Self motivation and ability to work independently

- A cooperative and team-oriented approach

- Candidates must be fluent in English language (both verbal and written)



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:



Labcorp Drug Development, Covance by Labcorp, Lead Statistical Programmer, Senior Statistical Programmer, Covance, Statistical programming, Chiltern, Covance, Phases I-IV, Programmer Analyst, Stats Programmer, Senior, Statistical Programmer, Lead SAS Programmer, CDISC, ADaM, SDTM, Biostatistics, Senior Statistician, Biostatistician, Statistics, Study Biostatistician, pharma, pharmaceutical, SAS, STAT, home based, pharma, pharmaceutical, home-based, flexible working, flexible location, home based, field based, home based EU Anywhere, anywhere in Europe, field-based, United Kingdom, UK, Great Britain, England, Maidenhead, Reading, Berkshire, Birmingham, Cambridge, Sheffield, Manchester, Alderley Edge, Scotland, Edinburgh, Wales, Swansea, Northern Ireland, Austria, Belgium, Bulgaria, Czech Republic, France, Paris, Germany, Greece, Hungary, Ireland, Italy, Lithuania, Netherlands, Leiden, Poland, Portugal, Romania, Russia, Slovakia, Bloemfontein, Centurion, South Africa, Madrid, Barcelona, Spain, Ukraine, oncology, cancer, #LI-PL1, #LI-Remote,  Remote, EMEA

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