Statistical SAS Programmer/Senior SAS Programmer/Principal SAS Programmer

What we are looking for

We are looking for a statistical SAS Programmer with at least 3 years’ experience (Senior or Principal roles available depending on experience) to join our Statistics and Programming team. SAS Base Certification is essential and Advanced Certification/ Clinical Trials Certification is desirable. You will have a graduate degree in Mathematics, Computer Science, Biostatistics/Statistics, Educational Measurement or equivalent experience in statistical SAS programming.. Experience of statistical analysis in SAS is essential, familiarity with creating macros also desirable. Analysis of COA data (particularly PROs) in observational and clinical trial data, preferably in a pharmaceutical company, healthcare research consultancy, contract research organisation or academic setting is highly desirable. Experience of clinical trials analysis would also be advantageous. For the senior/principal role knowledge of CDISC, SDTM and ADaM specifications and best industry practices and experience of working in a senior/principal capacity in a SAS programming environment are essential. Experience of training, mentoring and/or line management of more junior programmers is also desirable for the senior/principal role.

How you fit in

As a key member of our global Statistics and Programming team, you will join a vibrant group who partner with a broader team of qualitative researchers/PRO measurement specialists within the Patient-Centered Outcomes practice. You will be responsible for developing flexible SAS programs that analyse COA data from clinical trials and observational studies, in accordance with developed Statistical Analysis Plans (SAP) and best industry practices. You will leverage your knowledge and experience in the production of analysis datasets, tables, figures and data listings. Technical requirements include hands-on experience with PROC SQL, PROC REPORT, ODS OUTPUT, SAS macro language, and SAS/GRAPH. You will use statistical procedures such as PROC GLM, PROC LOGISTIC, PROC LIFETEST, PROC PHREG and PROC MIXED. You will also QC other programmers’ analytic datasets and outputs and employ QC/data exploration procedures such as PROC FREQ, PROC MEANS, PROC PRINT and PROC COMPARE. For the senior/principal roles you will be comfortable combining, transposing and merging several datasets that may be organised in a complicated manner (such as diary data).

Apply for this role
Send us your CV
Send us your CV



What we offer

We believe in rewarding high performance – so our benefits package includes a competitive salary, performance-related rewards, health insurance, pension, and gym membership. We provide support for further qualifications in a friendly and informal office environment. This position can be fully home-based or at our European head office, in a stunning location just outside Manchester, UK.

If you wish to join our team of enthusiastic and dedicated people, please email your CV and accompanying letter describing why you feel you are suitable for this role (SAS programmer/Senior/Principal as appropriate) to:

“I love the fast paced, highly challenging, and fun environment at Adelphi Values. I have learned a great deal and look forward to building upon my skill-set in the future.”

Research Associate, Patient-Centered Outcomes

To all recruitment agencies

Adelphi Values does not accept unsolicited agency resumes. Recruitment agencies should not send resumes to our HR team or to any of our employees. We are not responsible for any fees related to unsolicited resumes from recruitment agencies.

To all applicants

Legislation requires us to ensure that all candidates hold valid documents supporting their identity and their entitlement to work in the UK. At the time of starting their employment, the successful candidate must have permission to work in the UK.