Senior Global Trial Manager

IQVIA; São Paulo; Remote; BRL 601,000 - 820,000; Full time

Job summary

IQVIA is seeking a Senior Global Trial Manager to lead large, multi-regional clinical studies, with a focus on oncology. You will drive delivery, ensure regulatory compliance, and mentor cross‑functional teams in a fast‑paced environment.

This role involves travel up to 25% and a home-based work arrangement, with strong English communication and solid project management practices essential for success in global trials.

Qualifications

• Bachelor's Degree in health care or other scientific discipline (graduated).
• At least 7 years of experience in clinical research.
• Oncology experience is required.
• Solid global trial management experience.
• Advanced English level and good communication skills.
• Knowledge of GCP/ICH guidelines.
• Problem-solving, prioritization, attention to detail.

Responsibilities

• Provide clinical delivery of large, multi-regional studies in compliance with regulatory requirements.
• Lead clinical teams to deliver projects and manage internal and external stakeholders.
• Develop recruitment strategies and meet recruitment targets.
• Contribute to risk mitigation plans and manage clinical risks.
• Ensure clinical quality delivery and plan compliance measures.
• Oversee project finances, including Estimate at Completion (EAC).
• Provide training and mentorship to project staff.
• Travel up to 25% - home based position.

Skills

Global trial management

Oncology

Advanced English

Communication skills

Education

Bachelor's degree

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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