Associate Director, Statistical Programming - Remote

Overview

The Associate Director of Statistical Programming will lead a team to deliver high-quality statistical programming support for clinical trials and regulatory submissions in the pharmaceutical industry, ensuring compliance with industry standards and timelines.

In Short

• Oversee a team of statistical programmers.
• Ensure compliance with regulatory guidelines.
• Collaborate with cross-functional teams.
• Drive process improvement initiatives.
• Manage project timelines and budgets.
• Coordinate with external vendors as needed.
• Stay updated on industry trends and technologies.
• Provide mentorship and career development.
• Experience in oncology or cell therapy is preferred.
• Expertise in SAS programming is required.

Requirements

• Master’s degree or above in Statistics, Computer Science, or related field.
• 10+ years of statistical programming experience.
• 4+ years in a leadership role.
• Proven track record in clinical trials and regulatory submissions.
• Expertise in SAS (Base, Macro, SQL).
• Knowledge of CDISC standards (SDTM, ADaM).
• Experience with data visualization tools.
• Strong leadership and team-building skills.
• Excellent communication skills.
• Attention to detail and problem-solving skills.

Benefits

• Opportunity to work in a cutting-edge biotechnology company.
• Contribute to life-saving therapies.
• Collaborative work environment.
• Professional development opportunities.
• Competitive salary and benefits package.