Remote Clinical Trial Regulatory Advisor – Argentina

Syneos Health, Inc.; Argentina; Remote; ARS 139,474,000 - 201,463,000; Full time

Job summary

Syneos Health, Inc. seeks a Clinical Trial Regulatory Advisor to manage regulatory submissions for Canadian trials from a home-based position in Argentina. The role emphasizes compliance with GxP standards and cross‑functional collaboration on global teams.

You will review core documents, contribute to submission strategy, and ensure timely, high-quality deliverables across the study lifecycle. Strong English, communication, and teamwork are essential in this international, remote setup.

Qualifications

• Minimum of a BA or BS preferred.
• Experience in working to applicable GxPs (e.g. GVP, GCP, ISO 14155) etc.
• Excellent presentation, documentation, influencing, and interpersonal skills (both written and spoken English).
• Proficient computer skills in Microsoft Office Suite, web-based systems, voicemail, Email and Internet are necessary.

Responsibilities

• Provide regulatory and technical support for assigned regulatory work, review and finalise essential core documents, and manage submissions.
• Perform CTRA operations deliveries on specific project activities including regulatory leading functions to satisfy client requirements.
• Review study core documents (e.g., labeling for regulatory compliance) and prepare technical components of regulatory submissions.
• Contribute to agency interactions and support activities across the project lifecycle.
• Manage day-to-day regulatory activities for assigned projects within timelines, scope, budgets, and strategies.
• Serve as SME and assist team with day-to-day troubleshooting and problem-solving.

Skills

Regulatory knowledge

English proficiency

Stakeholder communication

Team collaboration

Education

Bachelor's degree

Tools

Microsoft Office

Job description

Syneos Health, Inc. seeks a Clinical Trial Regulatory Advisor to manage regulatory submissions for Canadian trials from a home-based position in Argentina. The role emphasizes compliance with GxP standards and cross‑functional collaboration on global teams.

You will review core documents, contribute to submission strategy, and ensure timely, high-quality deliverables across the study lifecycle. Strong English, communication, and teamwork are essential in this international, remote setup.