Statistical Programming Associate Director

Job Title: Statistical Programming Associate Director

Introduction to role

The Statistical Programming Associate Director is responsible for ensuring the quality, timeliness, and efficiency of project programming work and information management. This role requires extensive programming experience and industry knowledge to independently lead programming activities and supervise other programmers. It is a leadership position with a technical or project focus, providing subject matter expertise within the Programming field. As an expert, you will collaborate with cross-functional teams to foster continuous improvement.

Accountabilities

The role involves leading and directing the full scope of project delivery or managing a technical project within the TA/Drug Project/study/function. Key responsibilities include:

1. Implementing statistical programming aspects of protocols or clinical development programs.
2. Ensuring high quality of all project deliverables and holding partners accountable.
3. Leading or contributing to process improvement initiatives.
4. Developing and implementing best practices to enhance quality, efficiency, and effectiveness.
5. Establishing and enforcing standards.
6. Managing and escalating risks in complex or novel situations.
7. Providing programming expertise and tactical input to the team.
8. Supporting recruitment, training, and mentorship within the team.
9. Identifying opportunities for methodological improvements and practical problem-solving.
10. Managing external partners, such as Contract Research Organizations.
11. Influencing collaborators through subject matter expertise.
12. Ensuring compliance with standards and automation tools.
13. Applying project management practices to drug or technical projects.
14. Contributing to capacity planning for all projects.
15. Maintaining current knowledge of industry and regulatory requirements.

Essential Skills/Experience

Candidates should have:

• A degree in Mathematics, Statistics, Computer Science, Life Science, or equivalent.
• Proven programming expertise.
• Thorough knowledge of the clinical development process.
• Understanding of industry standards and their implementation.
• Problem-solving and troubleshooting skills.
• Up-to-date technical and regulatory knowledge.
• Ability to manage multiple activities proactively.
• Effective stakeholder influence skills.
• Risk management capabilities.
• A project-oriented mindset.

Desirable Skills/Experience

Additional desirable qualities include strong planning and organizational skills.

Our work environment emphasizes in-person collaboration at least three days a week, balanced with flexibility. We are committed to innovation, global collaboration, and continuous improvement, aiming to deliver life-changing medicines. Join us and make a meaningful difference in patients\’ lives!

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