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.