Senior Sas Programmer

Overview

• Contribute to pharmaceutical data analysis and reporting as a Senior SAS Programmer on a contract basis.
• Work remotely, leveraging your expertise in SAS programming to support clinical and regulatory projects.
• Engage in a dynamic role requiring senior-level experience and a strong analytical background.
• Collaborate with cross-functional teams to ensure data integrity and compliance with industry standards.
• Utilize your skills to contribute to impactful pharmaceutical research and development initiatives.
• Opportunity to work with cutting-edge technologies and methodologies in a remote setting.

Key Responsibilities & Duties

• Develop and validate SAS programs for clinical trial data analysis and reporting.
• Ensure the accuracy and consistency of datasets and outputs for regulatory submissions.
• Collaborate with statisticians and data managers to meet project objectives.
• Provide technical expertise in SAS programming and data manipulation techniques.
• Maintain compliance with industry standards and regulatory requirements in all programming activities.
• Document programming processes and outputs for audit and review purposes.
• Participate in team meetings to discuss progress and resolve technical challenges.

Job Requirements

• Bachelor of Science (BS) degree in a relevant field is required.
• Minimum of 5 years of experience in SAS programming, with 6 years preferred.
• Proficiency in clinical trial data analysis and regulatory submission standards.
• Strong knowledge of statistical programming and data manipulation techniques.
• Ability to work independently in a remote environment while meeting deadlines.
• Excellent communication skills for collaboration with cross-functional teams.
• Familiarity with industry standards such as CDISC and SDTM is advantageous.