Adelphi Values is a leading health outcomes consultancy that works with a wide range of pharmaceutical and medical device companies. In the Patient-Centered Outcomes practice we are global leaders in the selection, development, psychometric evaluation and use of Clinical Outcome Assessments (COA) including Patient-Reported Outcomes, Clinician-Reported Outcomes (ClinRO), Observer-Reported Outcomes (ObsRO) and Performance-Reported Outcomes (PerfO). We are a dedicated team of researchers who want to make meaningful difference and are proud of our high standards of scientific rigor and client service. We are a small team, where there is plenty of opportunity to influence decision making and develop leadership skills and we are committed to personal development, growing the individual through training and rewarding high performance. We are equally proud of our friendly, supportive culture and our approach to people and their working environment as we are of our reputation and high quality research which puts the patient at the centre of drug development.
We are looking to expand the Statistical and Programming Team with a statistical SAS Programmer at any level from three years’ experience upwards, including Senior and Principal roles depending on experience. The clinical data we analyse is diverse and sometimes complex compared to much clinical trials data. You will have a logical mind to unravel the detail in the data and enjoy the challenge of what at times requires intricate data manipulation. Programmers work closely with their statistics and psychometric colleagues in a small, tightly knitted team. SAS Base Certification is essential and Advanced Certification/ Clinical Trials Certification is desirable or equivalent experience. Experience of statistical analysis in SAS is essential, and 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. Some knowledge of R would be beneficial, as would further education involving statistics. For the role knowledge of CDISC, SDTM and ADaM specifications and best industry practices and experience of leading studies are essential. Experience of training, mentoring and/or line management of more junior programmers and developing and improving processes, including the creation of standard macros to be used across studies is also desirable for the role. You will have a graduate degree in Mathematics, Computer Science, Biostatistics/Statistics, Educational Measurement or equivalent experience in statistical SAS programming.
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 and figures. 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 role you will be comfortable combining, transposing and merging several datasets that may be organised in a complicated manner (such as diary data).