Associate Director - Statistics (Clinical Trial) - Remote

Overview

The Associate Director, Statistics provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs. The Associate Director works in partnership with experts in multiple disciplines to advance medicines to our patients.

In Short

• Provide statistical support for clinical development projects.
• Lead statistical strategy for project development and regulatory submission.
• Develop protocols and statistical analysis plans.
• Train and mentor staff on statistical methodology.
• Ensure compliance with regulatory requirements.
• Collaborate with other functions to create development strategies.
• Build external scientific connections for professional development.
• Critically review regulatory submission documents.
• Manage project timelines and quality of deliverables.
• Drive innovation and challenge the status quo.

Requirements

• MS or PhD in Statistics, Biostatistics, or Mathematics.
• 10+ years (MS) or 6+ years (PhD) of experience in clinical trials.
• Excellent communication skills, both oral and written.
• Able to identify data or analytical issues.
• Strong leadership skills and experience managing cross-cultural teams.
• Pharmaceutical or related industry knowledge required.
• Ability to build strong relationships with peers and partners.
• Expertise in innovative statistical methods.
• Experience with regulatory environments.
• Able to manage project timelines effectively.

Benefits

• Comprehensive benefits package including medical and dental insurance.
• Paid time off for vacation, holidays, and sick leave.
• Participation in short-term incentive programs.
• Opportunities for professional development.
• Support for recruiting qualified personnel.