Senior Global Trial Manager

IQVIA; Ciudad de México; Remote; MXN 2,620,000 - 3,556,000; Full time

Job summary

IQVIA is seeking a Senior Global Trial Manager to lead multi-regional clinical trials, ensuring regulatory compliance and high-quality delivery. You will guide global teams, optimize recruitment, manage risks, and oversee project finances while collaborating with stakeholders across functions.

The role requires Oncology experience, a strong background in clinical research, and excellent English communication skills. Travel up to 25% with a home-based arrangement is expected.

Qualifications

• Bachelor's degree in health care or other scientific discipline.
• At least 7 years of experience in clinical research.
• Oncology experience is required.
• Advanced English level with strong communication skills.
• Solid knowledge of regulatory requirements (GCP, ICH).

Responsibilities

• Ensure clinical delivery of assigned projects in compliance with regulatory requirements, customer contracts, and internal SOPs.
• Meet project recruitment targets and develop recruitment strategies.
• Contribute to project risk mitigation plans and manage clinical risks throughout the project lifecycle.
• Ensure clinical quality delivery by identifying quality standards and planning compliance measures.
• Manage clinical aspects of project finances, including Estimate at Completion (EAC).
• Lead clinical teams to deliver large, global trials and manage stakeholders.
• Support milestone achievements and reporting to stakeholders as per project scope requirements.
• Manage the clinical team at the project level, including resourcing and training.
• Travel up to 25% - home based position.

Skills

Clinical research

Oncology

Global trial management

English proficiency

Education

Bachelor's degree in health sciences

Job description

Buenos Aires, Argentina

Mexico City, Mexico

São Paulo, Brazil

Full time

R1576740

We 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.com

IQVIA 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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