Job Description
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Site Contracts Associate I - FSP based in the United States.
In this role, you will contribute directly to the successful activation of clinical trial sites by supporting the drafting, negotiation, and execution of essential site contracts. You will work at the intersection of legal, operational, and clinical teams to ensure agreements are accurate, compliant, and aligned with study requirements. The position plays a key role in enabling timely study start-up activities while maintaining strong relationships with research sites. You will be responsible for ensuring contract quality, regulatory compliance, and alignment with applicable laws and guidelines. Working in a collaborative and fast-paced clinical research environment, you will engage with both internal stakeholders and external partners. This role is ideal for detail-oriented professionals who enjoy negotiation, structured processes, and contributing to global clinical development efforts.
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Site Contracts Associate I - FSP based in the United States.
In this role, you will contribute directly to the successful activation of clinical trial sites by supporting the drafting, negotiation, and execution of essential site contracts. You will work at the intersection of legal, operational, and clinical teams to ensure agreements are accurate, compliant, and aligned with study requirements. The position plays a key role in enabling timely study start-up activities while maintaining strong relationships with research sites. You will be responsible for ensuring contract quality, regulatory compliance, and alignment with applicable laws and guidelines. Working in a collaborative and fast-paced clinical research environment, you will engage with both internal stakeholders and external partners. This role is ideal for detail-oriented professionals who enjoy negotiation, structured processes, and contributing to global clinical development efforts.
