Director

• Responsible for designing new programming standards and implementing them across the programming organization
• Take full ownership of existing shared codebases and automation frameworks
• Architect scalable reusable macro frameworks and modernize legacy code
• Ensure consistent, efficient, and compliant programming practices aligned with CDISC and regulatory expectations
• Collaborate with data management, statistics, clinical, and quality teams to ensure programming practices align with CDISC standards

Associate Director, Programming – Macros & Automation

• Lead management of strategic IT partner(s), ensuring their activities and deliverables are aligned with CSL’s business goals, service expectations and in-line with existing agreements/contracts.
• Build and maintain strong, collaborative relationships with strategic partners to drive mutual success and innovation.
• Act as the escalation point of contact and liaison between internal stakeholders and partners, facilitating clear communication, risk identification, issue resolution, and strategic alignment.
• Foster a culture of transparency, trust, and accountability to drive long-term partner engagement and performance.
• Manage and resolve disputes, perform escalations as needed, maintain an issue log and track disposition of issues (resolved, in-process, etc.)
• Facilitate measurement and reporting of strategic partner(s) performance based on contract SLAs and metrics, ensuring timely and accurate reporting.
• Drive strategic partner(s) incentives and penalties based on contractual requirements, supporting accountability and continuous improvement.
• Manage escalations and SLA breaches involving strategic partner(s), serving as the escalation point for performance, commercial, and delivery issues, in coordination with Procurement and Legal.

Director, PEO Partner Management

Software Engineer

• Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADaM datasets, Tables, Figures, Listings and Analysis Submission content.
• Plans and leads the production and validation efforts for the designed output, this may include oversight of work by CROs.
• Collaborates with study teams to ensure the quality and accuracy – thus submission readiness – of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml).
• Supports the review of related deliverables when provided by CROs.
• Leads and oversees requested efforts for pooled and exploratory analyses working closely with Statistics TA lead and/or study statisticians as well as with clinical programming team and their collection of legacy data.
• Leads and oversees the in-house specification and delivery of ISS and ISE datasets and associated output (tables, figures and listings) when not provided by CRO
• Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format.
• Leads and oversees the development of global tools that will increase the efficiency and capacity of the Statistical Programming group.
• Works closely with clinical study teams to execute activities to ensure project timelines are met with high quality deliverables.
• Additional tasks: Collaborates with CR&D staff regarding data analysis requests.

Principal Programmer

Research Scientist

• Provides scientific and clinical development input for the safe, efficient and timely execution of assigned programs, ensuring the highest quality and full compliance of all outputs
• Will contribute to the development of the scientific strategy of the clinical development plan, the design and development of trial related documents and the scientific oversight of clinical trials
• Facilitates a team to define and deliver the clinical strategy within projects and programs
• Defines scientific strategy for various program components
• Can lead development of Clinical Development Program
• Authors clinical study documents and assists with development/critical review of submission documents
• Contributes to authorship and review of manuscripts, conference abstracts, etc.
• Collaboratively develops the clinical development strategy with project teams, providing input, guidance and mentorship for project teams
• Contributes to the scientific analysis and interpretation of clinical data and the writing of clinical study reports, internal and external scientific meeting presentations and peer-reviewed publications, and all regulatory submission documents

Principal Scientist

AI Engineer

• Develop and execute a digital acceleration roadmap aligned with the broader R&D Technology Enabled Science vision.
• Identify, evaluate, and implement cutting-edge technologies (e.g., AI/ML, data analytics, automation, digital twin, cloud platforms) to support R&D activities.
• Partner with R&D teams to digitize key processes, enhance data utilization, and enable rapid experimentation.
• Lead the charge using Agentic Software Development approaches to drive innovation in R&D.
• Drive cultural and organizational change to support digital adoption, including change management and stakeholder engagement.
• Work closely with CSL I&T and R&D teams, as well as external partners and startups.
• Define KPIs and metrics to track the impact of digital initiatives on R&D productivity and outcomes.
• Hire, develop and retain critical talent, modernization our delivery and development methodologies to align to a platform delivery mindset.

Associate Director, Programming – Macros & Automation

Director, PEO Partner Management

Principal Programmer

Principal Scientist

Executive Director – R&D Advanced Analytics, Automation, AI Lead