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IQVIA

Senior Clinical Trial Manager – Oncology

IQVIA

. Lead and work alongside clinical teams to deliver full-service, large, multi-regional clinical studies .

Posted 10/22/2026full-timeCenturion • South AfricaSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in clinical trial management, ensuring compliance with regulatory standards such as GCP and ICH, while effectively managing project finances and stakeholder relationships. Proven ability to lead clinical teams, implement recruitment strategies, and deliver high-quality clinical studies across multiple regions.

Highest-signal resume keywords
Global CTM ExperienceClinical Trial ManagementRegulatory Compliance (GCP, ICH)Project Financial ManagementStakeholder Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Trial ManagementProject Management PracticesRegulatory Requirements KnowledgeClinical Research Industry UnderstandingProject Financial UnderstandingProtocol KnowledgeTherapeutic KnowledgeRisk Mitigation PlanningQuality Compliance MeasurementRecruitment Strategy Implementation
Soft Skills
Team LeadershipCommunicationMentoringCollaborationChange Advocacy
Industry Keywords
Clinical StudiesClinical OperationsClinical ResearchProject Lifecycle ManagementOperational PlansPerformance FeedbackSite VisitsBid DefensesCorporate InitiativesClinical Delivery Strategies

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Lead and work alongside clinical teams to deliver full-service, large, multi-regional clinical studies
  • Ensure clinical delivery complies with regulatory, customer, contractual, policy, SOP, and project-plan requirements
  • Meet project recruitment targets and implement appropriate recruitment strategies
  • Contribute to risk mitigation plans and manage clinical risks throughout the project lifecycle
  • Ensure clinical quality delivery by defining standards, measuring compliance, and overseeing quality issues
  • Manage clinical project finances, including EAC, scope, baselines, changes, and additional service opportunities
  • Work as the primary CTM alongside other CTMs on large, global trials
  • Identify and manage internal and external clinical stakeholders
  • Collaborate with clinical teams to achieve milestones and report to stakeholders
  • Plan resources and talent, manage the clinical team, and establish operational plans, guidance, and project training
  • Conduct team meetings and communicate to achieve objectives
  • Support professional development through performance feedback to clinical team line managers
  • Adopt corporate initiatives and act as a change advocate
  • Contribute to clinical delivery strategies for proposals, bid defenses, and Clinical Operations plans
  • Mentor and coach new peers
  • Attend site visits as applicable

Requirements

What you’ll need
  • Bachelor's Degree in health care or another scientific discipline required
  • Previous Global CTM experience required due to sponsor requirements
  • Ideally at least 5 years’ experience in clinical trial management or equivalent combination of education, training and experience
  • Consolidated knowledge of project management practices and terminology
  • Good knowledge of applicable clinical research regulatory requirements, including GCP and ICH guidelines
  • Broad protocol knowledge and therapeutic knowledge
  • Good understanding of the clinical research industry and relevant operating environments
  • Understanding of project finances
  • Knowledge of clinical trial conduct and ability to apply ICH, GCP, and relevant local laws, regulations, and guidelines