Clinical Research Coordinator providing assistance on clinical research studies including recruiting and organizing data. Supporting patient consent and clinical tests within a hybrid work setting.
About the role
- Intern providing statistical support for clinical trials in medical devices under supervision. Conduct data analysis, support clinical trials activities, and communicate statistical results clearly.
Responsibilities
- 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.
Job title
Job type
Experience level
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Not specified
Degree requirement
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