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IQVIA

Qualitative Project Manager, Patient Centered Solutions

IQVIA

. Ensure clinical delivery of assigned projects complies with regulatory, customer and internal requirements .

Posted 9/21/2026full-timeMexico City • MexicoMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in clinical project management, ensuring compliance with regulatory requirements and effective stakeholder communication. Proficient in clinical trial conduct, risk management, and financial oversight within the clinical research industry.

Highest-signal resume keywords
Clinical Research ExperienceRegulatory Compliance KnowledgeProject Financial ManagementStakeholder ManagementStrong Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Trial ConductRisk Mitigation PlanningProtocol KnowledgeGCP KnowledgeICH Guidelines KnowledgeProject Finances UnderstandingMicrosoft Office SkillsAttention to DetailTime ManagementProblem-Solving
Soft Skills
CollaborationInfluencing Without AuthorityCultural AwarenessPerformance FeedbackPrioritization
Certifications & Qualifications
Bachelor's Degree in Health Care or Scientific Discipline
Industry Keywords
Clinical ResearchRegulatory RequirementsClinical Quality IssuesOperational PlansRecruitment StrategiesClinical StakeholdersGlobal TrialsClinical DeliveryProject LifecycleClient Focus

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Ensure clinical delivery of assigned projects complies with regulatory, customer and internal requirements
  • Meet project recruitment targets and implement appropriate recruitment strategies
  • Develop project risk mitigation plans and manage clinical risks throughout the project lifecycle
  • Identify quality standards, plan compliance measurement, and oversee clinical quality issues
  • Manage clinical project finances, including Estimate at Completion (EAC), baseline changes and additional service opportunities
  • Identify and manage internal and external clinical stakeholders
  • Collaborate with clinical teams to achieve milestones and report to stakeholders
  • Plan resources and talent for clinical teams and establish operational plans, guidance and project training
  • Conduct team meetings and communicate to achieve objectives
  • Support professional development by providing performance feedback to clinical team line managers
  • Work as sole Clinical Lead on smaller projects or alongside senior Clinical Leads on large global trials
  • Attend site visits as applicable

Requirements

What you’ll need
  • Bachelor's Degree in health care or other scientific discipline required
  • Requires 3 years clinical research/monitoring experience or equivalent combination of education, training and experience
  • Requires good knowledge of applicable clinical research regulatory requirements, including GCP and ICH guidelines
  • Requires broad protocol knowledge and therapeutic knowledge
  • Requires good understanding of the clinical research industry and relevant operating environments
  • Requires basic understanding of project finances
  • Knowledge of clinical trial conduct and applicable clinical research regulatory requirements, ICH, GCP, and relevant local laws, regulations and guidelines
  • Strong written and verbal communication skills, including good command of English
  • Problem-solving skills
  • Planning, time management and prioritization skills
  • Ability to handle conflicting priorities
  • Attention to detail and accuracy
  • Microsoft Office skills, including Word, Excel and PowerPoint
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients
  • Ability to work across cultures and geographies with awareness and understanding of cultural differences
  • Ability to influence without authority
  • Ability to demonstrate IQVIA competencies: Client Focus, Collaboration, Communication, Innovation and Ownership