Programmer

Job Description

Responsibilities: –

• Develop, validate, and maintain SAS programs for clinical study deliverables.
• Generate and review Data Validation Listings (DVLs) to ensure data accuracy, completeness, and consistency.
• Support the creation and maintenance of clinical data outputs, reports, and listings.
• Apply programming best practices, including code optimization, documentation, and quality control.
• Collaborate with cross-functional teams including Data Management, Biostatistics, and Clinical Operations.
• Utilize SAS macros and SQL programming to automate and streamline processes.
• Participate in data review activities and contribute to issue resolution.
• Support study milestones and timelines while ensuring adherence to regulatory and company standards.

Required Qualifications: –

• Strong proficiency in SAS programming.
• Hands-on experience in developing and reviewing Data Validation Listings.
• Good understanding of clinical trial data and programming standards.
• Working knowledge of SAS Macros and SQL.
• Strong analytical, problem-solving, and communication skills.
• Demonstrated understanding of programming best practices and quality standards.

Preferred Qualifications: –

• Experience with Protocol Deviation Listings and Patient Profile generation.
• Knowledge of the Clinical Data Management (CDM) full lifecycle.
• Exposure to Power BI for data visualization and reporting.
• Experience working in regulated clinical research environments.

Desired Skills: –

• Clinical Data Programming
• SAS Base, SAS Macros, SQL
• Data Validation & Quality Control
• Protocol Deviations
• Patient Profiles
• Clinical Data Management (CDM)
• Power BI (Preferred)
• Team Collaboration & Stakeholder Communication

Are you interested in this position?
Apply by clicking on the “Apply Now” button below!
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