CK Group are recruiting for a RWE SAS Programmer, to join a global pharmaceutical company, based in Slough, on a contract basis initially for 12 months. This role can be fully remote.
Salary: 27.27 per hour Umbrella, 20.03 per hour PAYE (minimum - can go higher for more experienced candidates).
RWE SAS Programmer Role:
Supports Statistical programming activities in Real World Evidence. Provides input on study design and analysis plans where necessary. Develops, validates, maintains, and documents analysis programs and other study documents. Provides input on interpretation of results and reviews publications. Reviews the study concept, protocol design, analysis plans and other study-related documents.
Your Background: 5+ years experience in SAS programming. 2+ years experience in Real World Evidence, Epidemiology, or Health Outcomes environment. 2+ years experience with large health care databases such as CPRD or Merative MarketScan. Knowledge of R (preferable). Good study design and epidemiological and statistical analysis experience, including understanding of drug development, observational and epidemiological endpoints and assessments.
Company: Our client is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology now and into the future.
Location: Can be fully remote.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote reference (Apply online only).
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. #J-18808-Ljbffr
Salary: 27.27 per hour Umbrella, 20.03 per hour PAYE (minimum - can go higher for more experienced candidates).
RWE SAS Programmer Role:
Supports Statistical programming activities in Real World Evidence. Provides input on study design and analysis plans where necessary. Develops, validates, maintains, and documents analysis programs and other study documents. Provides input on interpretation of results and reviews publications. Reviews the study concept, protocol design, analysis plans and other study-related documents.
Your Background: 5+ years experience in SAS programming. 2+ years experience in Real World Evidence, Epidemiology, or Health Outcomes environment. 2+ years experience with large health care databases such as CPRD or Merative MarketScan. Knowledge of R (preferable). Good study design and epidemiological and statistical analysis experience, including understanding of drug development, observational and epidemiological endpoints and assessments.
Company: Our client is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology now and into the future.
Location: Can be fully remote.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote reference (Apply online only).
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. #J-18808-Ljbffr
