Global Site Activation Manager

Iqvia; Lima; On-site; ARS 185,966,000 - 278,949,000; Full time

Job summary

IQVIA is seeking a Senior Site Activation Leader to drive global activation strategies for clinical trials across regions. You will oversee site identification, regulatory submissions, contracting, and lifecycle operations to meet timelines and stay compliant with ICH-GCP standards.

Lead international projects, mentor teams, and manage budgets while collaborating with stakeholders to accelerate study start-up and enrollment. Requires 7+ years in clinical research with leadership experience.

Qualifications

• Bachelor's degree in Life Sciences or related field.
• Minimum 7 years clinical research experience with 3+ years in leadership role.
• Proven international project management across multiple regions.
• Strong leadership, negotiation, and stakeholder management skills.
• Demonstrated ability to deliver projects on time and within budget.

Responsibilities

• Provide strategic oversight and project management for global site activation activities.
• Lead site identification, regulatory submissions, contracting, and essential document processes.
• Develop and execute Site Activation Management Plans aligned with study strategy and timelines.
• Collaborate with internal teams and external stakeholders to ensure efficient study start-up execution.
• Mentor team members and maintain client relationships while supporting business development activities.

Skills

Leadership

Project management

Global coordination

Stakeholder mgmt

Regulatory knowledge

Education

Bachelor's degree in Life Sciences

Job description

Lead global site activation strategies across multiple regions to accelerate clinical trial enrollment. Manage site identification, regulatory submissions, contracting, and lifecycle operations while ensuring compliance with ICH-GCP standards and project timelines.

Responsibilities

• Provide strategic oversight and project management for global site activation activities
• Lead site identification, regulatory submissions, contracting, and essential document processes
• Develop and execute Site Activation Management Plans aligned with study strategy and timelines
• Collaborate with internal teams and external stakeholders to ensure efficient study start-up execution
• Mentor team members and maintain client relationships while supporting business development activities

Requirements

• Bachelor's degree in Life Sciences or related field
• Minimum 7 years clinical research experience with 3+ years in leadership role
• Proven international project management across multiple regions
• Strong leadership, negotiation, and stakeholder management skills
• Demonstrated ability to deliver projects on time and within budget
• Knowledge of regulatory requirements and clinical trial compliance