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IQVIA

Global Site Activation Manager

IQVIA

. Provide strategic oversight and project management for global or multi-regional Site Activation activities.

Posted 10/14/2026full-timeRemote • Argentina, Mexico, Chile, Peru, Brazil, ColombiaSeniorLeadWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in strategic oversight and project management for global Site Activation activities, ensuring compliance with ICH-GCP and regulatory requirements while delivering projects on time and within budget. Strong leadership capabilities are complemented by excellent communication and stakeholder management skills, fostering effective collaboration across teams and regions.

Highest-signal resume keywords
Project ManagementRegulatory ComplianceLeadership ExperienceStakeholder EngagementClinical Trial Expertise

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Site Activation ManagementRegulatory SubmissionsProject TrackingRisk AssessmentBudget ManagementQuality AssuranceClinical ResearchInternational Project ExperienceStrategic PlanningProblem Solving
Soft Skills
CommunicationNegotiationTeam DevelopmentCollaborationClient Relationship Management
Industry Keywords
ICH-GCPClinical TrialsLife SciencesRegulatory IntelligenceStudy StrategyBid DefenseContinuous ImprovementCross-Functional RelationshipsEssential Document ProcessesStudy Start-Up Execution

About the role

Key responsibilities & impact
  • Provide strategic oversight and project management for global or multi-regional Site Activation activities.
  • Lead start-up delivery from pre-award through activation and lifecycle maintenance in compliance with ICH-GCP, regulatory requirements, and project timelines.
  • Develop and execute the Site Activation Management Plan aligned with study strategy and scope of work.
  • Collaborate with internal teams, regions, and external stakeholders to ensure efficient study start-up execution.
  • Oversee regulatory submissions, approvals, contracts, and essential document processes.
  • Assess regulatory landscapes and contribute to regulatory intelligence and strategy.
  • Identify risks and propose practical solutions to support study delivery and bid processes.
  • Ensure accurate tracking, reporting, and maintenance of project systems, timelines, and documentation.
  • Support business development, including bid defense and client engagement activities.
  • Mentor and coach team members and contribute to continuous improvement initiatives.
  • Build and maintain strong client relationships and support customer-facing activities.

Requirements

What you’ll need
  • Bachelor’s degree in Life Sciences or related field.
  • Minimum 7 years’ experience in clinical research, including 3+ years in a leadership role.
  • Proven international project experience across multiple regions.
  • Strong leadership and project management skills with ability to manage multiple priorities.
  • Demonstrated ability to deliver projects on time, within scope, and budget.
  • Excellent communication, negotiation, and stakeholder management skills.
  • Ability to lead through others and maintain effective cross-functional relationships.
  • Strategic thinking and problem-solving.
  • Leadership and team development.
  • Regulatory and clinical trial expertise.
  • Stakeholder engagement and collaboration.
  • Quality and compliance focus.