Senior Biostatistician

April 15

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Clario

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Clario is a company specializing in accelerating clinical trials from initiation to implementation through advanced technologies and services. Since 2018, Clario has revolutionized endpoint analyses in clinical trials by integrating over 30 artificial intelligence-enabled solutions across more than 600 active trials, enhancing data quality and patient privacy while expediting data collection processes. Clario provides a comprehensive clinical trial management platform, offering solutions such as eCOA, cardiac safety, medical imaging, precision motion, and respiratory services in various therapeutic areas including oncology, cardiology, and neurology. Known for its global reach, Clario supports clinical trials in over 100 countries with a strong focus on decentralized and hybrid trial models. The company's commitment to patient safety and innovation is reflected in their over 26,000 trials and involvement in numerous new drug approvals.

Cardiac Solutions • Medical Imaging • eCOA • Respiratory Solutions • Precision Motion

1001 - 5000 employees

Founded 1973

⚕️ Healthcare Insurance

🧬 Biotechnology

🤖 Artificial Intelligence

💰 Private Equity Round on 2019-10

📋 Description

• Create, test and maintain SAS codes used to create and/or validate statistical outputs for cardiac safety analysis • Develop, test, execute and maintain SAS and R programs for statistical analysis • Validate results of statistical analysis by double programming • Prepare tables, figures, and listings for statistical analysis as outlined in the statistical analysis plan • Perform review of final outputs and reports • Support research programs and provide research results to senior team resources • Provide interpretation of results and reports of statistical analysis • Train team members on standard operating procedures and methodology • Develop process improvements to increase operational efficiency • Participate in Client discussions to communicate statistical methodologies • Work with cross-functional team to understand the scope of work for statistical deliverables

🎯 Requirements

• A PhD in Statistics, Mathematics or equivalent • A Master’s degree in Statistics, Mathematics or equivalent and 4+ years of relevant industry experience • Bachelor’s degree in Statistics, mathematics or equivalent with 10+ years of relevant industry experience • Familiarity and experience with ANOVA, t-test, regression, and linear mixed-effects modeling • Strong SAS or R programming skills • Experience in clinical trials within a CRO or pharmaceutical research organization • Familiarity with Clinical protocols and Statistical Analysis Plans, understanding of the pharmaceutical drug development process • Excellent verbal and written communication skills • Awareness of CDISC SDTM and ADaM standards • Strong organization, analytical and communication skills • Experience with Windows and Microsoft Office products • Experience with TFLs generation • Ability to learn quickly, function independently, and handle increasing levels of responsibility • Familiarity with Clario products and service lines • Previous experience in statistical modeling for clinical trials with focus on QT modeling • Ability to work in a group setting and independently, adjusting to rapidly changing priorities

🏖️ Benefits

• Competitive compensation + shift allowances • Attractive benefits (security, flexibility, support and well-being) • Engaging employee programs • Technology for hybrid working and great onsite facilities