Senior or Principal Statistical Programmer
hace 3 días
Cmed is seeking a Senior or Principal Statistical Programmer for this client dedicated opportunity. Multiple years of relevant late-stage clinical trial SAS statistical programming experience in analysis and reporting is required. Can be based remotely anywhere in Spain, Poland, or Romania.
Minimum 5 years for Senior Statistical Programmers or minimum 10 years for Principal Statistical Programmers.
Proficient SAS programming skills with mastery of SAS/STAT SAS/BASE, SAS macro language. SAS/GRAPH is a plus. SAS/MACRO is a must for this mission.
Capacity to interface with clinicians and statisticians as statistical programmer in charge of a clinical trial.
Capacity to work independently or under the guidance of a project lead statistical programmer.
Capacity to quickly read SAS code (including MACRO code) developed by others, understand them in the context of clinical trials and adjust to address the business question.
Knowledge and practice of CDISC SDTM and ADaM data standards. ADaM is a must have.
Ability to work complying to the company programming SOPs, project data standards and macro library as well as capacity to develop project specific code independently under company SOPs.
Strong and proven experience of work with clinical trial data in support of safety and efficacy analysis.
Able to contribute to the finalization of Programming Requirement Specifications based on study documents and mínimal guidance from the programming and statistics project leads.
Fast learner, team oriented, able to work independently.
Able to read, write and speak fluently in English. English writing skills are a must for this mission.
Experience with SAS on PC and UNIX platforms.
Oncology therapeutic area experience is an asset but not necessary as the person may work on other therapeutic areas.
Ability to function in a virtual team
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