Principal Statistician

Warman O'Brien; United States; Remote; USD 100,000 - 140,000; Full time

Job summary

Join a globally recognized pharmaceutical company as a Principal Biostatistician. You'll lead clinical programs, mentor teams, and ensure compliance with regulatory guidelines in a supportive, remote-friendly environment. Ideal for those with advanced statistical expertise and a passion for innovative drug development.

Qualifications

• 7+ years experience with a Ph.D. or 10+ years with a Master’s.
• Strong proficiency in statistical analysis and programming.

Responsibilities

• Oversee clinical trial programs ensuring statistical practices.
• Mentor biostatisticians and programmers in a collaborative team.
• Develop and implement Statistical Analysis Plans (SAPs).

Skills

Statistical Analysis

Leadership

Project Management

Strategic Thinking

Education

Ph.D. in Statistics

Master’s in Statistics

Job description

Direct message the job poster from Warman O'Brien

Become a key member of a globally recognized pharmaceutical company, where your statistical insights will power the development of life-changing therapies. We're looking for a driven Principal Biostatistician to lead impactful clinical programs and advance your career in a supportive, remote-friendly environment.

What will you be doing?

• Oversee clinical trial programs, driving operational efficiency and ensuring rigorous statistical practices.
• Mentor and develop biostatisticians and programmers, fostering a collaborative and growth-oriented team.
• Collaborate with multidisciplinary teams to design innovative protocols and contribute to strategic drug development decisions.
• Develop and implement Statistical Analysis Plans (SAPs), conduct complex statistical modelling, and ensure high-quality deliverables.
• Maintain compliance with regulatory guidelines, manage statistical quality control, and support regulatory interactions.

What do you bring to the table?

• Advanced degree (Ph.D. or Master’s) in Statistics or related field with significant experience (7+ years Ph.D., 10+ years Master’s).
• Strong proficiency in statistical analysis, programming, and regulatory requirements.
• Proven leadership abilities, project management skills, and strategic thinking.
• Desire to work in a collaborative and innovative remote environment.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Science, Analyst, and Research

Industries

• Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing