Senior Global Trial Manager

IQVIA; United States; À distance; USD 140 000 - 190 000; Plein temps

Résumé du poste

IQVIA seeks a Senior Global Trial Manager to lead multi-regional clinical trials, driving delivery and quality while ensuring regulatory compliance and sponsor requirements. You will guide global teams, manage risks, and optimize recruitment across studies from initiation to closeout.

The role requires oncology experience, strong English, and substantial clinical research background, with remote work in the United States and up to 25% travel to sites and stakeholders.

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.
• Previous experience in onsite monitoring activities.
• Solid global trial management experience delivering global trials.
• Advanced English level with strong communication skills.
• Knowledge of project management practices and terminology.
• Good knowledge of GCP and ICH guidelines.
• Excellent problem-solving skills and ability to manage conflicting priorities.
• Attention to detail and a results-oriented approach.
• Influencing, negotiation, judgment, and mentoring/training abilities.

Responsabilités

• Ensure clinical delivery of assigned projects in compliance with regulatory requirements, contracts, and SOPs.
• Meet recruitment targets and develop recruitment strategies.
• Contribute to project risk mitigation and manage clinical risks.
• Ensure clinical quality delivery by planning standards and addressing quality issues.
• Manage project finances, including EAC, and identify additional service opportunities.
• Lead clinical teams to deliver large, global trials and manage stakeholders.
• Support milestone achievements and reporting to stakeholders.
• Manage the clinical team at the project level, including resourcing and training.
• Travel up to 25% – home based position.

Connaissances

Global trial management

Oncology experience

Advanced English

Clinical research

Project management

Communication skills

Regulatory knowledge (GCP/ICH)

Problem solving

Attention to detail

Mentoring and training

Formation

Bachelor's degree in health care or scientific discipline

Description du poste

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.