Global Site Activation Manager

Location: Homebased in Buenos Aires, Argentina; other listed locations include Mexico City, Mexico; Santiago, Chile; Lima, Peru; São Paulo, Brazil; and Bogota, Colombia.

Company

Provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Lead strategic, operational, and financial delivery of global or multi-regional site activation activities.
• Manage study start-up from pre-award through activation and lifecycle maintenance in line with ICH-GCP, regulatory requirements, and project timelines.
• Develop and execute Site Activation Management Plans aligned with study strategy and scope of work.
• Oversee site identification and selection, regulatory submissions, approvals, contracts, essential documents, and project tracking.
• Assess regulatory landscapes, identify risks, and propose practical solutions for study delivery and bid processes.
• Support business development, client engagement, team mentoring, and continuous improvement initiatives.

Requirements

• Bachelor’s degree in Life Sciences or a related field.
• At least 7 years of experience in clinical research, including 3 or more years in a leadership role.
• International project experience across multiple regions.
• Strong leadership, project management, communication, negotiation, and stakeholder management skills.
• Ability to manage multiple priorities and deliver projects on time, within scope, and within budget.
• Expertise in regulatory and clinical trial requirements, quality, and compliance.

Culture & Benefits

• Home-based work arrangement.
• Opportunity to work with global and multi-regional clinical research programs.
• Cross-functional collaboration with internal teams, regions, clients, and external stakeholders.
• Focus on leadership development, mentoring, quality, compliance, and continuous improvement.