Senior Clinical Study Manager

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Clinical Study Manager based in United States.

This is a senior clinical research role focused on developing and executing studies that generate meaningful evidence for regulatory approvals and strategic clinical initiatives.

You will lead pre-market and post-market clinical studies with substantial autonomy, from study design and site selection through enrollment, follow-up, analysis, and reporting.

The role combines clinical operations, evidence strategy, scientific literature assessment, regulatory support, and cross-functional project leadership.

You will collaborate closely with investigators, key opinion leaders, CRAs, CTAs, biostatisticians, data management teams, vendors, and internal stakeholders.

Your work will directly contribute to high-quality clinical evidence, scientific publications, regulatory submissions, and improvements in clinical research strategy.

The environment is highly collaborative and technically rigorous, with opportunities to influence processes, mentor colleagues, and support studies across evolving surgical specialties.

This opportunity is well suited to an experienced clinical research professional who is organized, scientifically curious, self-directed, and comfortable managing complex studies and competing priorities.