Argentina-Based Hybrid Clinical Project Manager

Syneos Health/ inVentiv Health Commercial LLC; Morrisville (NC); Hybrid; USD 65,000 - 85,000; Full time

Job summary

Syneos Health is seeking a Project Specialist for a hybrid Argentina role. The candidate will plan and manage clinical study timelines, coordinate input from cross-functional teams, and ensure compliance with SOP/GCP across trials.

This role requires 3+ years in clinical project management, strong organizational skills, and proficiency with MS Office. The position offers hybrid work arrangements and a dynamic, collaborative environment.

Qualifications

• High school diploma or equivalent required.
• Associate’s degree or higher in a related field preferred.
• Minimum of 3 years of experience in clinical project management or a related field.
• Strong understanding of clinical trial processes and regulations.
• Experience with SOP, GCP, and country-specific regulations.

Responsibilities

• Planning, directing, creating, and communicating clinical study timelines, ensuring milestones are met.
• Gathering input from cross-functional teams to create plans for timely deliverables.
• Ensuring consistency of clinical study processes across trials by standardizing procedures.
• Overseeing and resolving operational aspects of clinical trials, including SOP/GCP compliance.
• Selecting sites and vendors for clinical trials, negotiating contracts, and managing relationships.
• Preparing clinical trial budgets, monitoring expenditures, and ensuring the study remains within budget.
• Monitoring progress of clinical trials, tracking KPIs, and addressing deviations.
• Developing trial recruitment strategies and monitoring enrollment progress.

Skills

Organizational skills

Time‑management

Communication

Team collaboration

MS Office

Problem solving

Education

High school diploma or equivalent

Associate’s degree or higher

Tools

Microsoft Office Suite

Job description

Syneos Health is seeking a Project Specialist for a hybrid Argentina role. The candidate will plan and manage clinical study timelines, coordinate input from cross-functional teams, and ensure compliance with SOP/GCP across trials.

This role requires 3+ years in clinical project management, strong organizational skills, and proficiency with MS Office. The position offers hybrid work arrangements and a dynamic, collaborative environment.