Are you a highly experienced Trial Statistician specialising in end-to-end clinical study design within pharmaceutical manufacturing? We're seeking a contract expert to join our team, driving statistical excellence from protocol development through to final reporting.

You'll be instrumental in shaping the statistical integrity of our trials, championing innovative designs and novel methodologies.

Key Responsibilities:

• Lead clinical study design and protocol development, providing expert statistical input.
• Drive statistical research and offer solutions for complex computational challenges.
• Oversee statistical deliverables and ensure compliance with company standards.
• Take primary responsibility for reporting and analysis execution across multiple studies.
• Mentor and guide junior statisticians, fostering a culture of excellence.
• Ensure statistical integrity of study reports, adhering to regulatory guidelines.
• Provide input on process improvement initiatives and participate in non-clinical project activities 
• Contribute to interactions with external review boards/ethics committees, external consultants, and other external parties with oversight as appropriate

Experience:

• Extensive experience (10 years plus) as a Statistician with a strong focus on end-to-end clinical study design in pharma manufacturing/biotech or CRO environment
• Proven ability to implement innovative trial designs.
• Excellent communication skills, able to explain complex statistics clearly.
• Strong leadership and a proactive approach.

This is a remote role in the USA, working with the EST timezone