Senior Global Regulatory Lead – Clinical Trials

7257 Syneos Health Argentina S.A.; Buenos Aires; Hybrid; ARS 139,018,000 - 200,803,000; Full time

Job summary

Syneos Health is seeking a Senior Clinical Trial Regulatory Advisor in Argentina to lead regulatory activities for submissions across countries. You will prepare core packages, manage CTIS submissions, and report on regulatory status to project teams and clients.

The role requires strong GxP knowledge, excellent communication, and the ability to manage complex timelines and risk assessments. This is a global opportunity to influence regulatory strategy within a leading life sciences partner,

Qualifications

• Bachelor’s degree or higher with strong regulatory knowledge and drug development experience.
• Experience with GxPs (e.g., GCP, ISO14155) and regulatory submissions.
• Excellent communication, presentation and stakeholder management skills.

Responsibilities

• Lead regulatory deliverables for country, region or global scope.
• Prepare submission strategies and manage CTIS documents.
• Coordinate regulatory assessments and liaise with sponsors and teams.
• Develop client relationships and provide regulatory guidance.

Skills

Regulatory expertise

Project management

Regulatory writing

Education

Bachelor’s Degree

Higher Degree Preferred

Job description

Syneos Health is seeking a Senior Clinical Trial Regulatory Advisor in Argentina to lead regulatory activities for submissions across countries. You will prepare core packages, manage CTIS submissions, and report on regulatory status to project teams and clients.

The role requires strong GxP knowledge, excellent communication, and the ability to manage complex timelines and risk assessments. This is a global opportunity to influence regulatory strategy within a leading life sciences partner,