Provide statistical support for clinical trials in medical devices under the direct supervision of a senior biostatistician.
Conduct data analysis for clinical trial publications under supervision and collaborate with internal and external partners.
Support and execute clinical trials activities for medical devices including: Clinical trial design and sample size calculations for Clinical Study Synopsis and Clinical Investigation Plans (protocols).
Input on effective data collection methods.
Statistical Analysis Plans (SAPs) with appropriate methodology and data presentation.
Interpretation and communication of data and statistical results, including Clinical Study Report (CSR) development.
Contribute to project management plans and meet deadlines.
Communicate statistical concepts and results clearly to non-statistical colleagues.
Requirements
University degree (BSc or higher) in Statistics, Biostatistics, Mathematics, Epidemiology or related field.
Strong fundamentals in probability and inference.
Hands-on experience with SAS and/or R.
Good written and verbal communication skills.
Organized, analytical, and able to follow documented procedures.
Ability to explain statistical concepts to non-statistical audiences.
Benefits
Valuing different backgrounds: LivaNova values equality and diversity.
Professional development opportunities.
Ensure proper documentation of all activities (traceability, data specifications, analysis validation) per internal procedures.
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