Clinical SAS programmer
Clinical SAS programmer
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1 Vacancy
Job Description
- Conduct statistical programming and analysis of clinical research studies.
- Provide programming support for publication efforts and regulatory submissions.
- Manage the timely creation review completion and delivery of statistical programming activities and deliverables for study projects.
- Perform acquisition and curation of data including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization.
- Document and implement programming endpoint algorithms across various projects.
- Review and provide feedback on Statistical Analysis Plans.
- Manage the end-to-end analytics of deliverables from data curation through final presentation which may include preparation for abstracts and manuscripts.
- Inform internal and external project team members of statistical programming requirements deliverable status and resource needs.
- Program clinical research data to facilitate ease of analysis for observational hypothesis-generating studies.
- Conduct exploratory analyses to support publication and abstract submissions.
- Communicate statistical results to stakeholders to ensure accurate interpretation.
- Masters degree or foreign equivalent in Biostatistics or a related field.
- 6 years of experience as a Statistical Programming Clinical Trial Analytics Intern or a related role within the public health biomedical or medical device industries.
- Proficiency in SAS Programming SAS Macros R/R Studio Clinical Trial Design and Data Analysis.
- Strong analytical and problem-solving skills with attention to detail.
- Ability to work collaboratively in a team environment and communicate effectively with cross-functional teams.
- Excellent organizational skills and the ability to manage multiple tasks and projects simultaneously.
Employment Type
Full Time
