You will lead with purpose, breaking down barriers to innovation in a more connected, compassionate world
Job Summary
You will lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
Responsibilities include design of studies, calculation of sample size and power, writing of statistical portions of protocol and statistical analysis plan, review of protocol and case report forms, analysis and interpretation of data, and preparation of relevant sections of regulatory submissions, reports, and manuscripts.
Medtronic offers a competitive Salary and flexible Benefits Package including health, dental, vision insurance, 401(k) plan with employer contribution and match, and paid time off.
Matching Summary
You will lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
Salary
Base: $143,200.00 - $214,800.00; Bonus/Equity: Eligible for Medtronic Incentive Plan (MIP); Benefits: Health, Dental, Vision, HSA, FSA, Life Insurance, LTD, Dependent Daycare FSA, Tuition Assistance, Simple Steps, 401(k) match, Paid Time Off, Paid Holidays, ESPP, EAP, Non-qualified Retirement Plan Supplement, Capital Accumulation Plan
Skills & Requirements
Must-have
Statistical study design
Clinical trial data analysis
Sample size and power calculation
Statistical analysis plan writing
Regulatory submission support
Advanced statistical methods
SAS or R programming
Nice-to-have
Intrinsic curiosity in medical research
Leadership in process improvements
Cross-functional collaboration
Adaptability to evolving healthcare needs
Key Requirements
Bachelor's degree with 7 years of statistical experience in clinical trials
Advanced degree with 5 years of statistical experience in clinical trials
8+ years experience in medical device or pharmaceutical industries
Experience in clinical studies from design through approval stages