CTMA

Clinical Trial Manager Associate | Brisbane, CA

Base Salary: $120k-$135k | Hybrid

This is a high-growth biotech leveraging a proprietary platform to unlock a new way of understanding how drugs interact within living systems. Backed by strong funding and a world-class team, they're advancing a pipeline aimed at tackling complex diseases that have been difficult to drug historically. It's an opportunity to be part of a company pushing the boundaries of discovery with a truly differentiated approach.

What You'll Lead

• Support global clinical trials end-to-end, partnering closely with global and regional study management teams to drive day-to-day execution.
• Independently manage key study operations including site communications, timelines, risk logs, and action tracking.
• Lead site start-up activities across multiple countries, coordinating with regulatory, start-up, and monitoring teams.
• Oversee TMF quality and inspection readiness, ensuring completeness and compliance at all times.
• Draft and manage essential study documents (e.g., monitoring plans, training materials, site communications) and support study meetings and vendor interactions.
• Track study performance (enrollment, site metrics, supplies, budgets) and collaborate cross-functionally to resolve issues and meet study milestones.

What You Bring

• Bachelor's degree with 3+ years of clinical trial experience.
• Strong understanding of clinical trial operations and regulatory requirements (ICH-GCP, FDA).
• Experience working on insourced/global clinical studies and understanding of in-house execution models.
• Solid oncology clinical trial experience preferred.
• Prior experience supporting global, multi-region trials.