Sr. Site Activation Specialist (North America team)

IQVIA seeks a senior site activation specialist based in Argentina or Brazil to coordinate clinical trial site preparation activities across North American studies. The role involves managing documentation, regulatory compliance, and communication between investigative sites and internal teams.

Responsibilities

• Serve as single point of contact for assigned studies, coordinating between sites, activation managers, and project teams
• Execute feasibility, site identification, startup, and activation activities per regulations and standard procedures
• Prepare, review, and distribute site documents ensuring completeness and accuracy
• Maintain internal systems and databases with project-specific information
• Track and follow up on document approvals, regulatory submissions, ethics approvals, and ICF release timelines

Requirements

• Bachelor's degree in life science or related field
• 3+ years of clinical research experience in site activation or regulatory tasks
• Advanced English proficiency; fluency in global collaboration required
• Based in Argentina or Brazil
• Experience with site feasibility assessments and regulatory documentation