Senior/principal Programmer
3 weeks ago
We are currently looking for a Senior/Principal Programmer to join a leading Biopharmaceutical company based in the Oxfordshire area. As the Senior/Principal Programmer you will be responsible for Clinical Development, Enterprise Data & Analytics, or QDSprojects, ensuring all aspects of Programming activities supporting the success of those projects, including guidance, decision-making, and contributions to milestone planning and delivery, data and knowledge stewardship, and inspection readiness.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Senior/Principal Programmer will be varied however the key duties and responsibilities are as follows:
1. Provide SAS programming leadership to internal and external study teams in the reporting of clinical trials data, regulatory submissions, safety updates and publications.
2. Develop and review dataset specification documentation, dataset programs and associated reporting programs (tables, figures and listings) while following the clinical study protocol and/or statistical analysis plan.
3. Develop expert knowledge of CDISC methodology, specifically SDTM and ADaM models.
4. Ensure quality control is preformed on all programs written and is adequately documented.
ROLE REQUIREMENTS:
1. Substantial experience in the biotechnology and/or pharmaceuticals industries.
2. Substantial statistical and/or scientific programming experience in a life sciences environment using SAS (especially BASE, STAT, GRAPH), R, and/or other relevant programming languages.
Key Words: Senior, Principal, Programmer, SAS, Biopharmaceutical, Statistical, BASE, STAT, GRAPH, R, SDTM, ADaM ,
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