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: Competitive.
RWE SAS Programmer Role:
Support Statistical programming activities in Real World Evidence. Provide input on study design and analysis plans where necessary. Develop, validate, maintain, and document analysis programs and other study documents. Provide input on interpretation of results and review publications. Review 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 job reference 113 284.
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. #J-18808-Ljbffr
Salary: Competitive.
RWE SAS Programmer Role:
Support Statistical programming activities in Real World Evidence. Provide input on study design and analysis plans where necessary. Develop, validate, maintain, and document analysis programs and other study documents. Provide input on interpretation of results and review publications. Review 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 job reference 113 284.
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. #J-18808-Ljbffr
