Clinical Trials Project Coordinator

Syneos Health, Inc.; Buenos Aires; Hybrid; ARS 60,582,000 - 98,446,000; Full time

Job summary

Syneos Health, Inc. in Buenos Aires is seeking a Project Associate, RWLP to support planning and execution of clinical trial elements under the Project Lead. You will coordinate internal resources, monitor timelines and budgets, and help maintain financial reports.

With strong communication and analytical skills, you will drive risk management, document scope and decisions, and contribute to ensuring quality and regulatory readiness across study activities.

Responsibilities

• Drives the planning and execution of elements of clinical trials in partnership with the Project Lead.
• Ensures projects adhere to strict timelines and are delivered within budget.
• Coordinates internal resources and third parties/vendors for the efficient execution of projects.
• Conducts ongoing analysis of project performance to drive the successful completion of short and long-term goals.
• May maintain and distribute study-specific financial reports and contribute to study's financial health using financial processes and systems.
• Documents project scope and objectives, involving all relevant stakeholders.
• Leads communication between project team members, ensuring all parties are informed of project status and changes.
• Documents and escalates project risks and issues and drives timely follow-through and completion.
• Maintenance of systems and project management tools and methodologies.
• Drives quality assurance activities, including preparation for audits and internal review, prepare documentation and follow through to resolution on actionable issues.

Job description

Syneos Health, Inc. in Buenos Aires is seeking a Project Associate, RWLP to support planning and execution of clinical trial elements under the Project Lead. You will coordinate internal resources, monitor timelines and budgets, and help maintain financial reports.

With strong communication and analytical skills, you will drive risk management, document scope and decisions, and contribute to ensuring quality and regulatory readiness across study activities.