Senior Manager, Statistical Programming , Remote

AbbVie Inc; United States; Remote; USD 100,000 - 150,000; Full time

Job summary

An established industry player is seeking a Senior Manager for Statistical Programming to oversee oncology clinical projects. This pivotal role involves leading programming activities, managing a team, and ensuring high-quality data analysis. With a focus on SAS programming and adherence to CDISC standards, you will play a crucial part in delivering innovative solutions that address serious health issues. Join a dynamic team where your expertise will help shape the future of healthcare and make a remarkable impact on patients' lives.

Qualifications

• 9+ years of experience in statistical programming or 11+ years with a BS.
• Minimum 2 years leading a statistical programming team.

Responsibilities

• Lead statistical programming activities for oncology clinical trials.
• Manage a team of statistical programmers and ensure quality deliverables.

Skills

SAS Programming

Statistical Analysis

CDISC Standards

Team Leadership

Communication Skills

Education

Master's in Statistics

Bachelor's in Statistics

Tools

SAS

Job description

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn, and TikTok.

Job Description

The Senior Manager, Statistical Programming, performs oversight of statistical programming and analysis for Oncology Early Development (OED) clinical projects conducted by CROs. This role involves managing multiple compounds/indications, ensuring data integrity and high-quality analysis for oncology trials from first-in-human studies through clinical proof of concept. The individual also conducts hands-on programming to validate datasets and TLFs and may manage other statistical programmers.

Responsibilities include:

1. Leading statistical programming activities for specific compounds or therapeutic areas.
2. Managing a team of statistical programmers and resource planning.
3. Ensuring timely, quality deliverables following all processes and maintaining consistency.
4. Developing SAS programs for ADaM data sets following CDISC standards.
5. Developing SAS programs for Tables, Listings, and Figures.
6. Ensuring consistency across studies and data sets.
7. Creating documentation for regulatory submissions.
8. Leading development of SAS macros and SOPs.
9. Managing, mentoring, and developing staff careers.
10. Participating in recruitment and hiring processes.

Qualifications

• MS in Statistics, Computer Science, or related field with 9+ years of relevant experience, or BS with 11+ years.
• Minimum 2 years leading a statistical programming team.
• Deep understanding of SAS programming, CDISC standards, and drug development processes.
• Strong communication skills and ability to represent the organization in cross-functional teams.

Key Stakeholders include Directors of Statistics, Data Scientists, Medical Writers, Regulatory Publishers, and Clinical Project Managers.

Additional Information

This section details pay ranges, benefits, incentive programs, and legal disclosures relevant to applicants in applicable locations. AbbVie is an equal opportunity employer committed to diversity and inclusion. For more information or accommodations, visit the provided URLs.