
Investigator Contracts Lead I - FSP
Job Description
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for an Investigator Contracts Lead I – FSP based in Brazil.
This role plays a key part in enabling the successful initiation of global clinical trials by managing site contracting and budget negotiations with investigative sites.
You will act as a primary liaison for contract and budget discussions, ensuring alignment between clinical timelines, legal frameworks, and site expectations.
The position requires strong coordination across legal, finance, CRO partners, and clinical operations teams in a highly matrixed global environment.
You will lead study-level contracting activities, supporting both internal stakeholders and external research sites throughout the start-up phase.
A key focus is balancing risk, compliance, and operational efficiency while ensuring timely execution of clinical trial agreements.
You will also contribute to process improvements and escalation management across contracting workflows.
This is a high-impact role where negotiation expertise and cross-functional collaboration directly accelerate clinical development timelines.
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for an Investigator Contracts Lead I – FSP based in Brazil.
This role plays a key part in enabling the successful initiation of global clinical trials by managing site contracting and budget negotiations with investigative sites.
You will act as a primary liaison for contract and budget discussions, ensuring alignment between clinical timelines, legal frameworks, and site expectations.
The position requires strong coordination across legal, finance, CRO partners, and clinical operations teams in a highly matrixed global environment.
You will lead study-level contracting activities, supporting both internal stakeholders and external research sites throughout the start-up phase.
A key focus is balancing risk, compliance, and operational efficiency while ensuring timely execution of clinical trial agreements.
You will also contribute to process improvements and escalation management across contracting workflows.
This is a high-impact role where negotiation expertise and cross-functional collaboration directly accelerate clinical development timelines.