Clinical Trial Manager

ICON; United States; Remote; USD 70,000 - 110,000; Full time

Job summary

Join an innovative organization as a Clinical Study Manager, leading cutting-edge clinical studies in lab diagnostics. You will be at the forefront of advancing healthcare, ensuring compliance and quality while managing global teams. This role offers the chance to collaborate with diverse stakeholders and contribute to impactful research. The company values a diverse culture, providing various benefits focused on well-being and work-life balance. If you are passionate about clinical research and looking to make a difference, this opportunity is perfect for you.

Benefits

Annual leave entitlements

Health insurance options

Retirement planning options

Global Employee Assistance Programme

Life assurance

Flexible benefits

Qualifications

• Experience leading global clinical studies.
• Strong understanding of GCP, ICH, and clinical lab standards.

Responsibilities

• Manage global study teams, overseeing design, timelines, and budget.
• Develop and report on study protocols ensuring compliance.
• Collaborate with internal teams and external stakeholders.

Skills

Leadership

Communication

Problem-solving

Clinical study management

Regulatory compliance

Education

Bachelor's degree in medical technology

Bachelor's degree in chemistry

Bachelor's degree in biology

Tools

Microsoft Office

Job description

As a Study Manager, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. We are seeking a Clinical Trial Manager with experience managing IVD studies involving Core LAB or Pathology.

What you will be doing:

Lead and manage clinical studies that advance innovation in lab diagnostics. As a Clinical Study Manager, you will be responsible for planning, executing, and reporting on technical, clinical utility, and clinical performance studies, ensuring compliance, quality, and adherence to timelines.

1. Manage global study teams, overseeing study design, timelines, and budget

2. Develop, execute, and report on study protocols

3. Maintain data integrity, oversee database closure, and ensure regulatory compliance

4. Collaborate with internal teams, external stakeholders, vendors, and study sites

5. Support regulatory approval processes and publication activities

You Are:

• Bachelor's degree in medical technology, chemistry, biology, or related field

• Experience leading global clinical studies

• Strong communication, leadership, and problem-solving skills

• Proficiency in Microsoft Office; statistical knowledge is a plus

• Deep understanding of GCP, ICH, and clinical lab standards

What ICON can offer you:

Our success depends on the quality of our people. We prioritize building a diverse culture that rewards high performance and nurtures talent.

In addition to a competitive salary, ICON offers various benefits focused on well-being and work-life balance for you and your family, including:

• Annual leave entitlements

• Health insurance options

• Retirement planning options

• Global Employee Assistance Programme, TELUS Health, providing 24/7 access to support professionals

• Life assurance

• Flexible, country-specific benefits such as childcare vouchers, gym discounts, travel passes, and health assessments

Visit our careers website to learn more about working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental. We are committed to providing an inclusive, accessible environment and a workplace free of discrimination and harassment. Qualified applicants will be considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. If you need a reasonable accommodation during the application process or to perform essential job functions, please let us know at:

https://careers.iconplc.com/reasonable-accommodations

Interested but unsure if you meet all requirements? We encourage you to apply — you might be exactly who we’re looking for, whether for this role or others at ICON.