Principal Biostatistician

Responsibilities:

• Lead the development and implementation of statistical analysis plans (SAPs) for clinical trials and research studies, ensuring adherence to regulatory guidelines and industry standards.
• Collaborate with clinical operations, data management, and programming teams to ensure high-quality data collection, cleaning, and analysis.
• Oversight and review of vendor statistical activities, with accountability for study level timeliness and quality of deliverables.
• Provide statistical insight and exploratory analyses of completed and ongoing studies
• Communicate progress and identify risks and issues arising on clinical trials

Requirements:

• 5 years experience of clinical biostatistics in the pharmaceutical/biotech industry
• Experience managing outsourced biostatistics activities
• Programming experience with SAS
• In depth knowledge of GCP and related regulatory standards
• Independent, self starter with a proactive, problem-solving approach
• Excellent oral and written communication skills
• Ability to see complex projects to completion and work on broad range of tasks within a project

Additional information

• 2 days a week in Cambridge office / flexibility for remote work
• 75-95k salary

If you feel like you are ready for a new challenge and meet the requirements for this role. Please apply directly or feel free to reach me on my email: harrison.antino@albionryeassociates.com or call me on +44 20 33 71 92 56 for more information.