Job Description:
• The Principal Biostatistician is responsible for providing statistical support for drug development programs in early phases.
Requirements:
• Collaborate with multi-disciplinary project teams to establish project timelines.
• Provide statistical input to study protocols.
• Writes the statistical sections of clinical trial protocols, while consulting with internal and external experts.
• Write statistical analysis plans.
• Monitor internal and CRO project activities including timelines, deliverables, and availability of resources.
• Collaborates with Data Management, Clinical Development, and Clinical Operations with statistical expertise.
• Contributes to clinical study reports and other regulatory documents e.g., DSURs, Briefing Documents, etc.
• Provide guidance and supervision to programmers in authoring of analysis dataset specifications and programming of tables, listings, and figures.
• Interpret study results and review reports of study results for accuracy.
• Participate and contribute to authoring of Clinical Development Plan.
• Support exploratory analyses and medical affairs publications.
• Participate in pre-IND and NDA activities.
• Participates in other activities and meetings to support Biostatistics and the Development Team as needed.
Benefits:
• Home-based remote working opportunities
• Work/life balance as well as flexible schedules
• Collaborating with motivated, high-performance, statistical and research teams
• Technical training and tailored development curriculum
• Research opportunities that match your unique skillset
• Promising career trajectory
• Job stability: long-term engagements and re-deployment opportunities
• Focus on bringing new therapies to market rather than project budgets and change orders.
• Experience with regulatory submissions.
• Engaging, fast-paced environment.
• Good work-life balance.
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