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Job Description & How to Apply Below
Take charge as a Principal Biostatistician leading statistical initiatives in Oncology and CNS trials. Collaborate with cross-functional teams to deliver high-quality statistical outputs that meet regulatory standards.
In this senior role, the Principal Biostatistician provides oversight on numerous statistical projects. With a minimum of 7 years in the Pharma/Biotech industry, you will leverage your expertise in CDISC, FDA, and ICH regulations to drive project success. Your leadership will guide the statistical methodologies and ensure compliance with established standards.
Key Responsibilities:
• Act as the lead Biostatistician and project manager
• Interface with sponsors for requirements and timelines
• Author Statistical Analysis Plans and reports
• Manage ADaM package development and reviews
• Recommend methodologies for clinical trial analyses
Requirements:
• MSc. or PhD. in Biostatistics or Statistics
• 7+ years in Biostatistics in Pharma/Biotech
• Experience with CDISC, SDTM, and ADaM
• Strong communication and teamwork abilities
• Proven leadership in statistical project execution
Utilize your deep knowledge in statistics to enhance clinical trial quality and drive groundbreaking research outcomes.
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