Senior Biostatistics Lead, Clinical Development

AbbVie Inc.; Chicago (IL); On-site; USD 180,000 - 240,000; Full time

Benefits offered by this job

Paid time off (vacation, holidays, and

Medical/dental/vision insurance

401(k)

Job summary

AbbVie's Associate Director, Statistics provides statistical leadership for clinical development and lifecycle management strategies across assigned projects. You will partner with experts from Clinical, Regulatory, Patient Safety, and GMA to advance medicines to patients.

You will design, analyze, and report statistical studies, mentor staff, and contribute to publications. This role involves collaboration with CROs and external partners and supporting regulatory discussions as needed.

Qualifications

• MS or PhD in Statistics/Biostatistics or related field with required years of experience.
• Strong leadership and cross-cultural or overseas team management experience.
• Pharmaceutical industry knowledge including drug development and lifecycle management.
• PhD preferred
• Submission experience preferred

Responsibilities

• Provide statistical leadership for clinical development and lifecycle management strategies for assigned projects.
• Lead design, analysis and reporting for clinical or scientific research programs.
• Collaborate with Clinical, Regulatory, Patient Safety, and GMA to develop development strategies.
• Mentor staff on statistical methodology and operations; supervise junior statisticians.
• Develop data presentation and inference strategies; ensure accuracy of reports and publications.
• Liaise with CROs and external partners; support regulatory discussions as needed.

Skills

Leadership experience

Cross-cultural / global teamwork

Statistical leadership

Communication skills

Education

MS in Statistics/Biostatistics or related field

PhD in Statistics/Biostatistics or related field

Tools

SAS

R

Job description

AbbVie's Associate Director, Statistics provides statistical leadership for clinical development and lifecycle management strategies across assigned projects. You will partner with experts from Clinical, Regulatory, Patient Safety, and GMA to advance medicines to patients.

You will design, analyze, and report statistical studies, mentor staff, and contribute to publications. This role involves collaboration with CROs and external partners and supporting regulatory discussions as needed.