Principal Stat Prog Lead

Principal I Stat Prog Lead at Johnson & Johnson Innovative Medicine

Join us to apply for the Principal I Stat Prog Lead role. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Our expertise in Innovative Medicine and Med Tech positions us uniquely to deliver breakthroughs that profoundly impact health for humanity.

• Data Analytics & Computational Sciences
• Biostatistics
• Scientific/Technology

High Wycombe, Buckinghamshire, United Kingdom

The Principal Statistical Programming Lead is a highly experienced Statistical Programmer with expert knowledge of Statistical Programming languages, tools, and data structures. This individual leads Statistical Programming activities and teams in accordance with departmental processes, overseeing planning, oversight and delivery of statistical programming activities for high complexity/criticality projects and submissions.

This position is accountable for the planning, oversight, and delivery of statistical programming activities in support of one or more clinical projects, compounds and/or submissions generally of high complexity/criticality. It also leads and/or contributes expert knowledge and technical skills to therapeutic area and/or departmental innovation and process improvement projects. The role requires high degree of autonomy, decision making, and providing leadership, direction and technical guidance to programming teams.

• Accountable for Statistical Programming team delivery for high complexity projects.
• Provides matrix leadership to programming teams, coordinating and overseeing activities, and may act as a section lead.
• Contributes to strategic decisions, develops and maintains detailed programming strategy and plans.
• Provides technical and project‑specific guidance ensuring high quality and timely deliverables in compliance with departmental processes.
• Designs and develops programs and technical solutions for complex clinical research analysis and reporting activities, including urgent/on‑demand analysis requests.
• Applies technical and analytical expertise to develop and implement solutions for use on clinical projects, improving efficiency and quality.
• Champions adoption of new processes & technology on projects in collaboration with departmental technical groups and portfolio leads.

• Advanced Analytics
• Biostatistics
• Clinical Data Management
• Compliance Management
• Critical Thinking
• Data Privacy Standards
• Good Clinical Practice (GCP)
• Organizing
• Presentation Design
• Program Management
• Quality Assurance (QA)
• Regulatory Affairs Management
• Research Documents
• Standard Operating Procedure (SOP)
• Statistical Analysis Systems (SAS) Programming
• Survey Design

• Advanced Analytics
• Biostatistics
• Clinical Data Management
• Collaborating
• Compliance Management
• Critical Thinking
• Data Privacy Standards
• Good Clinical Practice (GCP)
• Organizing
• Presentation Design
• Program Management
• Quality Assurance (QA)
• Regulatory Affairs Management
• Research Documents
• Standard Operating Procedure (SOP)
• Statistical Analysis Systems (SAS) Programming
• Survey Design

Not Applicable

Full-time

Education and Training;
Pharmaceutical Manufacturing

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Salary: £28,000.00-£28,000.00