Statistical Programmer

Location
Poland
Salary
Negotiable
Posted
12 Jan 2021
Closes
11 Feb 2021
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Description Provide programming expertise and hands on technical support to clinical projects, across all phases and therapeutic areas as required by the client. Ensure a quality product is delivered, and excellent customer care provided at all times. Tasks and Responsibilities • Provide SAS programming support to internal and external study teams in the reporting of clinical trials data, regulatory submissions, safety updates and publications. • Develop dataset specifications, dataset programs and associated reporting programs (tables, figures and listings), while following the clinical study protocol and/or statistical analysis plan. • Ensure quality control is performed on all programs written and is adequately documented. • All programs written must follow good programming practise and be audit ready. • Review and provide input to case report forms, statistical analysis plans and associated table shells. • Develop expert knowledge of CDISC methodology, specifically SDTM and ADaM models. • Create tools or processes to improve programming efficiency and quality. • Work closely with internal or external study team and deliver consistently high quality results to agreed timelines. • Perform the role of Project Lead, Technical Lead and / or key client contact as required. • Mentor programmers within the department as required. • Perform any other reasonable tasks as requested by CEO / Operations Director. Minimum qualifications and experience • Bachelor’s degree or higher • Excellent oral and written communication skills. • Excellent analytical skills

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