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

This remote role supports the delivery of high-quality safety services across clinical research and medical device programs.
You will contribute to the accurate management, review, analysis, and reporting of individual case safety reports and clinical safety data.
The position also supports Clinical Events Committees (CECs), Data Monitoring Committees (DMCs), and related study safety activities.
You will collaborate with sponsors, study teams, regulatory stakeholders, and internal experts to maintain data quality and compliance.
The role combines hands-on safety case processing with quality assurance, documentation, reporting, and process improvement.
You will work in a collaborative, detail-oriented environment where sound judgment, organization, and regulatory awareness are essential.
This is an opportunity to contribute to clinical programs that support the development of innovative medical technologies and improved patient outcomes.

What the job really is