Senior Statistical Programmer
1 day ago
**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 (PII-IV) group with the opportunity to work across **multiple Sponsors and therapeutic areas**:
- Office based or home based anywhere in Europe or South Africa
- You must have previous experience of working as a Statistical Programmer in either a biotech, CRO or pharma company
Join our growing team and discover your extraordinary potential by working as a **Labcorp Drug Development **Senior Statistical Programmer. **You will work in our Clinical Development Services 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 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**:
- 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 SDTM and ADaM datasets and TFLs, and perform QC of SDTM, ADaMs and TFLs
- Produce Define XML/PDFs, Analysis Results Metadata (ARM), annotated CRFs and Reviewers Guides to support SDTMs and ADaMs
- Develop specifications for SDTMs and ADaM datasets
- Review SAPs and TFL shells from a programming perspective for studies
- Mentor less-experienced programmers in the processes around SDTMs, ADaMs and TFLs
- Present and share knowledge at department meetings
- Respond to QA and client audits, and support qualification audits
- Identify processes within programming that will increase productivity, quality and efficiency
**Job Qualifications**:
- You must have some previous experience of working as a Lead Statistical Programmer in either a biotech, CRO or pharma company using SAS.
- Knowledge of CDISC requirements
- 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
Are you passionate about improving health and improving lives? Then #JoinThePursuit.
**MORE INFORMATION AVAILABLE ON REQUEST**:
For a confidential discussion about this opportunity, please phone Peter Lewis on
+447917710602
. To apply, please click on the APPLY button.
NO AGENCIES PLEASE
**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
**Labcorp is proud to be an Equal Opportunity Employer**:
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