Remote Senior Statistical SAS Programmer Job in Maidenhead, UK CompuGain

Who you are

• Degree in a relevant field such as mathematics life sciences statistics computer sciences or an equivalent completed vocational training and / or equivalent professional experience in statistical programming for clinical trials.
• Solid professional experience as a statistical programmer within a biotech CRO or pharmaceutical company.
• Demonstrated knowledge of base SAS SAS macros SAS/STAT and demonstrated ability to debug SAS programs.
• Proven professional experience with SDTMs ADaM datasets (safety and efficacy) and TFLs.
• Solid knowledge of CDISC standards.
• Prior experience working on oncology data (safety and efficacy) and/or on vaccine trials.
• Submission experience is ideal.
• Strong organizational skills an autonomous and collaborative work style a curious mind and a keen attention to detail.
• Business fluency in English – both spoken and written – is a must.

Desirables

• Autonomous
• Collaborative work style
• Curious mind
• Attention to detail

What the job involves

• Lead studies through various phases of the clinical development plan and support submissions regulatory questions publications as well as ad hoc and post hoc requests.
• Develop and validate SAS programs for data presentations and analyses.
• Provide programming support to a multidisciplinary global project team.
• Participate in the development of innovative Oncology drugs.
• Improve the health and lives of thousands of patients around the globe every day.