Remote Principal Statistician, Clinical Trials & Regulatory

Medtronic; Mounds View (MN); On-site; USD 146,000 - 220,000; Full time

Benefits offered by this job

Health, Dental and Vision insurance

Tuition assistance/reimbursement

401(k) plan with company match

Employee Stock Purchase Plan

Job summary

Medtronic seeks a Principal Statistician to lead statistical design and analysis for complex clinical studies supporting regulatory submissions. You will write SAPs, review CRFs, and provide data interpretation across multi-disciplinary teams.

You will also oversee statistical support for FDA discussions, develop innovative methods, and drive standardization across the department while ensuring data integrity and quality.

Qualifications

• Bachelor's degree required.
• 7+ years of statistical experience in clinical trial design and data analysis in healthcare.
• Advanced degree with 5+ years of stat experience in healthcare.

Responsibilities

• Design and analyze biostatistical components of studies for regulatory submissions.
• Lead development of statistical analysis plans and protocol sections.
• Collaborate with clinical and programming teams to ensure data integrity.

Skills

Biostatistics

Statistical analysis

FDA/regulatory knowledge

SAS and R

Clinical trial design

Data interpretation

Education

Bachelor's degree

Advanced degree in Biostatistics or Statistics

Tools

SAS

R

Job description

Medtronic seeks a Principal Statistician to lead statistical design and analysis for complex clinical studies supporting regulatory submissions. You will write SAPs, review CRFs, and provide data interpretation across multi-disciplinary teams.

You will also oversee statistical support for FDA discussions, develop innovative methods, and drive standardization across the department while ensuring data integrity and quality.