Global Site Activation Manager

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