biotechnology • innovation • great place to work • pharmaceuticals • research and development
10,000+
September 24
biotechnology • innovation • great place to work • pharmaceuticals • research and development
10,000+
• Collaborates in design of innovative and efficient clinical trials • Defends protocols and analysis plans at internal governance reviews • Independently authors and/or reviews protocol, statistical analysis plan, clinical study reports • Presents summary data and analyses results • Provides statistical support and leadership to address health authority requests • Manages multiple studies to ensure consistency and adherence to standards • Applies extensive knowledge of statistical / clinical trials methodology • Effectively engages as a matrix team member on project teams • Contributes to external and internal statistical community of practice • Provides leadership to empower and develop the team
• PhD (6+ years’ experience) or MS (8+ years’ experience) in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience • Proficiency in scientific computing/programming (SAS, R or Python) and implementation of advanced statistical analysis, data manipulation, graphing & simulation • Great interpersonal, communication, writing and organizational skills • Expertise in statistical/clinical trials methodology as it relates to clinical development and ability to apply to relevant clinical development framework • Good understanding of regulatory landscape and experience with participating in regulatory interactions • Demonstrate collaboration, organizational/leadership abilities, and interpersonal skills • Demonstrate ability to plan, organize, and prioritize multiple work assignments, and strong project management skills • People manager experience is preferred (for people manager position only)
• Competitive benefits, services, and programs provided to employees to pursue goals
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