
Senior Programmer Analyst
Posted Aug 6

Posted Aug 6
This is a fully remote position, open to applicants in Argentina, +1 more state.
• Conduct advanced bioinformatics programming tasks related to statistical and computational aspects of research projects.
• Operate independently as the lead programmer for selected moderately complex studies.
• Participate as a study team member under the supervision of a lead programmer for more complex studies.
• Develop, execute, maintain, and validate SAS programs.
• Facilitate data transfer across various data management systems or operating systems.
• Integrate data from diverse sources and structures.
• Produce and archive summary data, reports, listings, tables, and figures.
• Assume the role of lead programmer for selected studies of moderate complexity.
• Collaborate with project team leaders and client representatives to establish project goals and timelines.
• Contribute to multidisciplinary clinical trials project teams.
• Oversee and document assignments to ensure adherence to timelines and quality standards.
• Conduct quality control reviews for statistical programming.
• Stay informed about contractual obligations and limitations.
• Provide training and mentorship to junior team members.
• Support departmental infrastructure, including conferences, meetings, training materials, documents, policies, working practices, and SOPs.
• Assist in the bidding process as required.
• MS/MA degree in Computer Science, Statistics, Biostatistics, Mathematics, or a related field, with a minimum of 3 years of relevant experience.
• Bachelor’s degree in Computer Science, Statistics, Biostatistics, Mathematics, or a related field, or an equivalent and relevant formal academic/vocational qualification, with at least 5 years of relevant experience.
• Necessary knowledge, skills, and abilities to fulfill job requirements.
• Proficiency in SAS programming.
• Capability to create, execute, maintain, and validate programs that generate listings, tables, and figures.
• Ability to transfer and integrate data across multiple systems, operating systems, sources, and structures.
• Understanding of programming technology and techniques, clinical trials, and the pharmaceutical industry.
• Competence in leading moderately complex studies.
• Ability to provide training and mentorship to junior team members.
• Skill in training and mentoring others.
• Competitive salary and compensation package.
• Opportunities for professional development and advancement.
• Comprehensive health and wellness benefits.
• Collaborative and inclusive work environment.
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