Global Clinical Trial Manager

PRA International; United States; Remote; USD 80,000 - 120,000; Full time

Job summary

A leading clinical research organization is seeking a Global Clinical Trial Manager to oversee clinical trials, ensuring adherence to regulations and timely delivery of milestones. The role requires significant experience in clinical trial management and a strong educational background in life sciences.

Benefits

Competitive total rewards package

Continuous learning opportunities

Comprehensive benefits

Qualifications

• At least 4 years of clinical trial experience, including 2 years in global clinical trial management.
• Experience in life sciences, biopharmaceutical research, especially in biotech or CRO settings.

Responsibilities

• Lead, manage, and coordinate the conduct of clinical trials at a global level.
• Ensure compliance with ICH-GCP, international regulations, and sponsor SOPs.
• Proactively communicate study status and manage risks.

Skills

Communication

Interpersonal Skills

Risk Management

Project Coordination

Education

BA/BS/BSc or RN degree

Job description

Overview

As a Global Clinical Trial Manager, you will play a key role in improving patients' lives by accelerating the development of our clients' drugs and devices through innovative solutions. You will be a dedicated resource embedded in a client's environment, systems, and processes.

Responsibilities

What you will be doing:

• Lead, manage, and coordinate the conduct of clinical trials from design to close-out at a global level, ensuring compliance with ICH-GCP, international regulations, and sponsor SOPs.
• Collaborate with Clinical Program Management teams for global study execution.
• Implement effective risk management strategies across all study areas.
• Maintain the quality and scientific integrity of global clinical operations.
• Work with internal and external stakeholders to ensure timely and within-budget delivery of clinical trial milestones.
• Proactively communicate study status, risks, mitigation plans, and issue resolutions to ensure on-time and on-budget study completion.

Qualifications

You are:

• Holding a BA/BS/BSc or RN degree.
• Having at least 4 years of clinical trial experience, including 2 years in global clinical trial management.
• Experienced in life sciences or related fields, with general biopharmaceutical research experience, ideally in biotech, pharmaceutical, or CRO settings.
• Possessing excellent communication and interpersonal skills for cross-functional teamwork.
• Knowledgeable of ICH/GCP guidelines and regulatory requirements.

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Benefits of Working in ICON

We are committed to developing our employees through continuous learning, engaging work, and professional growth. Our competitive total rewards package includes base pay, variable pay, recognition programs, and comprehensive benefits supporting you and your family throughout your career. ICON is an equal opportunity employer, providing a workplace free from discrimination and harassment. If you require reasonable accommodations during the application process or to perform your duties, please inform us.