Statistical Programming Associate Director

The Statistical Programming Associate Director is accountable for quality, timely and efficient delivery of project programming work and good information management. This position requires profound programming experience and excellent industry knowledge to independently lead implementation of programming activities as well as lead other programmers. It is a leadership role that can have a project or technical focus It will provide subject matter expertise within the Programming discipline. As an expert within their own field, acts as a specialist within cross-functional teams to deliver continuous improvement.

Leads and directs the full scope of project delivery and/or leads a technical project within the TA/Drug Project/study/function Leads Implementation of statistical programming aspects of the protocol or clinical development program

Responsible for the high quality of all project deliverables, holding partners and providers accountable for the quality of their deliverables and/or technical subject matter expert for aspect(s) of TA, Project, or function Leads or contribute to cross-functional administrative or process improvement initiative(s) Drives the development of best practices to improve quality, efficiency and/or effectiveness within the function Drives standards development and implementation Manages and escalate risk in complicated or novel situations within their study and/or projects Provides Programming expertise to the team Provides tactical input and/or drives ideas and improvements Contributes to the function by supporting recruiting and/or providing training and mentorship Identifies opportunities to improve methodology and provides practical solutions for problems Manages activities of our external partners (i.e. Contract Research Organisations) Influences stakeholders by providing subject matter expertise on programming related items Ensures compliance to standards and automation usage Employs all project management practices in managing drug or technical projects Provides input to capacity management for all projects in scope Maintains expertise of the latest industry and regulatory requirements to stay current

Leads or contribute to cross-functional administrative or process improvement initiative(s)

Drives the development of best practices to improve quality, efficiency and/or effectiveness within the function

Drives standards development and implementation

Manages and escalate risk in complicated or novel situations within their study and/or projects

Provides Programming expertise to the team

Provides tactical input and/or drives ideas and improvements

Contributes to the function by supporting recruiting and/or providing training and mentorship

Identifies opportunities to improve methodology and provides practical solutions for problems

Manages activities of our external partners (i.e. Contract Research Organisations)

Influences stakeholders by providing subject matter expertise on programming related items

Ensures compliance to standards and automation usage

Employs all project management practices in managing drug or technical projects

Provides input to capacity management for all projects in scope

Maintains expertise of the latest industry and regulatory requirements to stay current

Here you will contribute to a bold mission to transform outcomes for people by advancing earlier detection and smarter, faster trials. You will operate at the intersection of innovative science and technology, backed by significant investment and an empowered, collaborative culture that brings clinicians, scientists, and data experts together to accelerate breakthroughs. We value kindness alongside ambition, giving you the trust, tools, and cross-functional partnerships to lead with confidence and shape studies that matter—so your decisions today translate into meaningful patient impact tomorrow.

Step into this country leadership role to accelerate life-changing trials and turn bold science into result that matter—make your move and help shape what comes next.

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.