Senior Study Start-Up Specialist

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

This role is responsible for driving high-quality clinical study start-up activities from site selection through activation.
You will coordinate submissions, essential documentation, and start-up deliverables while ensuring milestones are achieved efficiently.
The position combines operational ownership, regulatory awareness, document management, and close collaboration with clinical research stakeholders.
You will help accelerate site activation timelines by leveraging established site relationships and identifying opportunities to reduce cycle times.
The role also contributes to improving local workflows, systems, and study start-up infrastructure across North America.
You will work in a collaborative clinical operations environment where attention to detail, clear communication, and proactive problem-solving are highly valued.
This is an opportunity to make a direct impact on the timely initiation of clinical studies while supporting compliant and consistent execution.