Senior Global Trial Manager

IQVIA Inc; Buenos Aires; Remote; ARS 139,474,000 - 232,457,000; Full time

Job summary

IQVIA Inc. seeks a Senior Global Trial Manager to lead multi-regional clinical studies from Buenos Aires or other major hubs, with travel up to 25%.

You will lead global trial delivery, oversee clinical teams, ensure regulatory compliance, and partner with stakeholders to drive on-time drug development. Oncology focus and strong English communication are required.

Join IQVIA to shape trial strategies, mitigate risks, and collaborate across Latin American sites and global teams.

Qualifications

• Oncology experience required for clinical trial leadership.
• Experience in onsite monitoring activities and global trial management.

Responsibilities

• Ensure clinical delivery of assigned global multi-regional trials in compliance with regulatory and internal SOPs.
• Lead clinical teams, manage resourcing, and coordinate stakeholders across sites.
• Develop recruitment strategies, manage budgets, and monitor risk throughout the project lifecycle.

Skills

Global trial mgmt

GCP compliance

ICH guidelines

Education

Bachelor's Degree in health care or science

Job description

Senior Global Trial Manager### Senior Global Trial ManagerApply: Buenos Aires, Argentina: Mexico City, Mexico: São Paulo, Brazil: Full time: Posted Yesterday: R1576740We are seeking a **Senior Global Trial Manager** to join our team! We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As a Global Trial Manager, you will play a crucial role in clinical trial delivery, leading clinical teams to bring new drugs to market faster. You will be responsible for the clinical delivery of large, multi-regional studies, ensuring compliance with regulatory, customer, and internal requirements. **What you’ll be doing:*** Ensuring clinical delivery of assigned projects in compliance with regulatory requirements, customer contracts, and internal SOPs.* Meeting project recruitment targets and develop appropriate recruitment strategies.* Contributing to project risk mitigation plans and manage clinical risks throughout the project lifecycle.* Ensuring clinical quality delivery by identifying quality standards, planning compliance measures, and managing clinical quality issues.* Managing clinical aspects of project finances, including Estimate at Completion (EAC), and identify additional service opportunities.* Leading clinical teams to deliver large, global trials and manage internal and external stakeholders.* Supporting milestone achievements and reporting to stakeholders as per project scope requirements.* Managing the clinical team at the project level, including resourcing, talent planning, and providing project-related training.* **Travel up to 25% - home based position.** **What we are looking for:*** 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, with effective mentoring and training abilities.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.