Position Overview:
We are seeking an experienced statistician to work primarily with SAS and clinical data. In this role, you will be responsible for analysing complex datasets, supporting clinical trials, and providing statistical expertise to drive our research initiatives.
Key Responsibilities: Analyse clinical trial data using SAS to generate meaningful insights and support decision-making. Collaborate with cross-functional teams, including researchers, clinicians, and data managers, to design and analyse clinical studies. Develop and validate statistical models to ensure the accuracy and reliability of study results. Prepare statistical analysis plans, reports, and presentations for internal and external stakeholders. Ensure compliance with regulatory requirements and industry standards in all statistical activities. Stay current with advancements in statistical methodologies and software tools. Qualifications: Master’s or PhD in Statistics, Biostatistics, or a related field. Minimum of 3 years of experience in statistical analysis, preferably in a clinical research setting. Proficiency in SAS programming and experience with clinical data. Strong understanding of statistical methodologies and their application in clinical trials. Excellent problem-solving skills and attention to detail. Effective communication skills, with the ability to present complex statistical concepts to non-statistical audiences. What We Offer: Competitive salary and benefits package. Opportunities for professional growth and development. A collaborative and innovative work environment. Flexible working hours and remote work options.
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Key Responsibilities: Analyse clinical trial data using SAS to generate meaningful insights and support decision-making. Collaborate with cross-functional teams, including researchers, clinicians, and data managers, to design and analyse clinical studies. Develop and validate statistical models to ensure the accuracy and reliability of study results. Prepare statistical analysis plans, reports, and presentations for internal and external stakeholders. Ensure compliance with regulatory requirements and industry standards in all statistical activities. Stay current with advancements in statistical methodologies and software tools. Qualifications: Master’s or PhD in Statistics, Biostatistics, or a related field. Minimum of 3 years of experience in statistical analysis, preferably in a clinical research setting. Proficiency in SAS programming and experience with clinical data. Strong understanding of statistical methodologies and their application in clinical trials. Excellent problem-solving skills and attention to detail. Effective communication skills, with the ability to present complex statistical concepts to non-statistical audiences. What We Offer: Competitive salary and benefits package. Opportunities for professional growth and development. A collaborative and innovative work environment. Flexible working hours and remote work options.
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