Programming Manager

📋 Description

• Serve as a skilled programmer across various clinical studies.

• Assist in activities related to regulatory submissions.

• Generate and validate datasets and outputs.

• Program and validate datasets and SDTMs.

• Create complex non-efficacy outputs and figures.

• Conduct Senior Review and ensure quality control of non-statistical outputs.

• Coordinate and execute code reviews.

• Develop, quality check, and revise intricate dataset specifications.

• Take on the role of Lead programmer for multiple studies and projects.

• Establish archiving systems and related processes.

⛳️ Requirements

• Holds a BSc or higher in Computer Science, Mathematics, or a related scientific field.

• Experience in SAS programming within the pharmaceutical sector.

• Strong understanding of clinical trial challenges, design, and execution.

• Familiarity with regulatory submissions and relevant industry guidelines.

• Knowledge of GCP and regulatory standards.

• Understanding of SDTM and ADaM CDISC standards.

🏝️ Benefits

• Opportunities for professional growth and development.

• Commitment to equal employment opportunities.

• Support for workforce diversity.