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IQVIA

Senior Global Trial Manager

IQVIA

. Ensure clinical delivery of assigned projects in compliance with regulatory requirements, customer contracts, and internal SOPs .

Posted 11/3/2026full-timeRemote • Argentina, Mexico, BrazilSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates extensive experience in clinical research management, particularly in oncology, with a strong focus on regulatory compliance, project delivery, and team leadership. Proven ability to manage clinical project finances and develop effective recruitment strategies while ensuring high-quality standards.

Highest-signal resume keywords
Clinical Research ManagementOncology ExperienceGlobal Trial DeliveryRegulatory Compliance (GCP, ICH)Project Management Practices

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical DeliveryProject Recruitment StrategiesRisk Mitigation PlansClinical Quality StandardsEstimate at Completion (EAC)Onsite Monitoring ActivitiesGlobal Trial ManagementProject Management Terminology
Soft Skills
Problem-SolvingAttention to DetailInfluencing SkillsNegotiation SkillsMentoring Abilities
Industry Keywords
Clinical ResearchRegulatory RequirementsStakeholder ManagementClinical Quality IssuesTalent Planning

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Ensure clinical delivery of assigned projects in compliance with regulatory requirements, customer contracts, and internal SOPs
  • Meet project recruitment targets and develop appropriate recruitment strategies
  • Contribute to project risk mitigation plans and manage clinical risks throughout the project lifecycle
  • Ensure clinical quality delivery by identifying quality standards, planning compliance measures, and managing clinical quality issues
  • Manage clinical aspects of project finances, including Estimate at Completion (EAC), and identify additional service opportunities
  • Lead clinical teams to deliver large, global trials and manage internal and external stakeholders
  • Support milestone achievements and report to stakeholders according to project scope requirements
  • Manage the clinical team at the project level, including resourcing, talent planning, and providing project-related training

Requirements

What you’ll need
  • Bachelor's Degree in health care or other scientific discipline (graduated)
  • At least 7 years of experience in clinical research
  • Oncology experience is required
  • Previous experience in onsite monitoring activities
  • Solid global trial management experience is required, responsible for global trial delivery
  • Advanced English level, and good communication skills in the language
  • Consolidated knowledge of project management practices and terminology
  • Good knowledge of applicable clinical research regulatory requirements (GCP, ICH guidelines)
  • Problem-solving skills and the ability to handle conflicting priorities
  • Attention to detail and accuracy in work, with a results-oriented approach
  • Good influencing, negotiation, judgment, and decision-making skills
  • Effective mentoring and training abilities

Benefits

Comp & perks
  • Travel up to 25%
  • Home based position