Senior I Statistical Programming Team Lead Position
6 days ago
We are seeking an experienced Senior I Statistical Programming Lead to join our team at Johnson & Johnson. As a key member of our statistical programming team, you will be responsible for leading analysis and reporting activities, as well as programming teams in accordance with departmental processes and procedures.
About the JobThe Senior I Statistical Programming Lead is an experienced Statistical Programmer with advanced knowledge of statistical programming methods, languages, and data structures. This position is accountable for the planning, oversight, and delivery of statistical programming activities supporting one or more clinical projects, compounds, and/or submissions of low-medium complexity/criticality.
As a leader, you will make decisions and recommendations that impact the efficiency, timeliness, and quality of deliverables. You will provide leadership, direction, and technical and project-specific guidance to programming teams.
Key Responsibilities- Accountable for Statistical Programming team delivery for one or more clinical projects generally of low to medium complexity, scope, or criticality.
- Coordinates and supervises programming team activities and provides technical and project-specific mentorship to programming team members to ensure quality and timely statistical programming deliverables in compliance with departmental processes and procedures.
- Develops detailed programming strategy, specifications, and plans the programming deliverables for a one or more clinical projects. May act as a section lead of programming activities supporting a clinical program, compound, or submission.
- Performs comprehensive review of, and provides input into, project requirements and documentation.
- Collaborates optimally with statistical programming and cross-functional team members and counterparts to achieve project goals.
- As applicable, coordinates statistical programming activities outsourced to third-party vendors adopting appropriate processes and methods to ensure their performance meets the agreed-upon scope, timelines, and quality.
- Bachelor's degree or higher and/or equivalent in computer science, mathematics, data science/analytics, public health, or other relevant scientific field (or equivalent theoretical/technical depth). Approximately 6-8 years programming experience with growing responsibility, preferably in a pharmaceutical/clinical trial environment.
- Advanced knowledge of relevant statistical programming languages including SAS (required), other relevant programming languages (e.g., R, Python, etc.) (preferred), and data structures.
- Proven experience planning and coordinating programming activities and leading teams.
- Proven experience working with cross-functional stakeholders and teams.
- Solid understanding of regulatory guidelines (e.g., ICH-GCP) and relevant clinical RD concepts.
- Basic project management skills.
- Demonstrated written and verbal communication skills.
The estimated annual salary for this role is $120,000 - $150,000, depending on experience and qualifications. We offer a competitive benefits package, including medical, dental, and vision insurance, 401(k) matching, and paid time off.
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