Senior Statistician
Senior Statistician
Your Role
- Serve as the lead statistician for at least one study within our clinical development programs, offering strategic statistical input from trial design to analysis.
- Collaborate with cross-functional teams on study design, including sample size, randomization procedures, endpoint selection, and case report form design.
- Develop, oversee, and ensure the alignment of Statistical Analysis Plans (SAPs) with study objectives and regulatory compliance.
- Oversee CRO deliverables, ensuring the accuracy, quality, and integrity of statistical outputs, including the production of tables, listings, and figures.
- Foster collaborative relationships within the clinical department and with external vendors to maintain effective communication and project integrity.
- Provide comprehensive statistical support across all phases of clinical trial and project development, including the design of clinical study reports.
Your Profile:
Requirements:
- A Master’s degree in statistics or a related field, with at least 5 years of relevant experience in clinical trial analysis.
- Demonstrated expertise in statistical analysis within clinical or related subjects – experience in oncology is a plus.
- Familiarity with international standards (ICH, GCP, CDISC) and clinical study regulations.
- Proficiency in statistical software packages (e.g., SAS, R).
- Excellent communication and interpersonal skills, with the ability to translate complex statistical concepts for non-technical audiences.
- Strong leadership and collaboration skills, capable of working on multiple projects simultaneously and under pressure.
Benefits
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