Related skills
r sas ngs biostatistics jmp📋 Description
- Drive design and execution of analyses for analytical validation studies.
- Support CLIA LDT and regulatory pathways (IVDR, 510(k), PMA).
- Perform stats analyses: sample size, power, agreement, LoD.
- Create presentations and document analysis plans, methods, results.
- Explain statistical results to cross-functional teams.
- Identify risks and propose solutions to project teams.
🎯 Requirements
- Master's in biostatistics or related field with 3+ years; or PhD with 1+ year.
- 2+ years' experience with statistical software such as R (preferred), SAS, or JMP.
- Experience in a regulated environment is a plus.
🎁 Benefits
- Medical, dental, vision, life and disability coverage.
- Free testing for employees and dependents; fertility care benefits.
- Pregnancy/baby bonding leave and 401k benefits.
- Commuter benefits and employee referral program.
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