Clinical Trial Manager

Lensa; United States; On-site; USD 100,000 - 145,000; Full time

Job summary

A leading clinical research organization is seeking a Clinical Study Manager to lead and manage clinical studies that drive innovation in lab diagnostics. You will be responsible for planning, execution, and reporting of studies, ensuring compliance and quality. The ideal candidate will have a Bachelor's degree in a related field and experience in leading global clinical studies.

Benefits

Various annual leave entitlements

A range of health insurance offerings

Competitive retirement planning offerings

Global Employee Assistance Programme

Flexible country-specific optional benefits

Qualifications

• Experience leading global clinical studies.
• Proficient in Microsoft Office; statistical knowledge a plus.
• Deep understanding of GCP, ICH, and clinical lab standards.

Responsibilities

• Lead global study teams with full ownership of study design, timelines, and budget.
• Oversee protocol development, execution, and reporting.
• Ensure data integrity, database closure, and compliance with regulatory standards.

Skills

Leadership

Problem-Solving

Communication

Education

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

Tools

Microsoft Office

Job description

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Lensa is the leading career site for job seekers at every stage of their career. Our client, ICON Clinical Research, is seeking professionals. Apply via Lensa today!

As a Study Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. We are looking for a Clinical Trial Manager who has managed IVD studies with Core LAB or Pathology experience!!

What You Will Be Doing

Join our global team to lead and manage clinical studies that drive innovation in lab diagnostics. As a Clinical Study Manager , you'll be accountable for the planning, execution, and reporting of technical, clinical utility, and clinical performance studies—ensuring compliance, quality, and timelines.

• Lead global study teams with full ownership of study design, timelines, and budget
• Oversee protocol development, execution, and reporting
• Ensure data integrity, database closure, and compliance with regulatory standards
• Collaborate with internal and external stakeholders, managing vendors and study sites
• Support regulatory approvals and publication plans
  
  

You Are

• Bachelor's in medical technology, chemistry, biology, or related field
• Experience leading global clinical studies
• Strong communication, leadership, and problem-solving skills
• Proficient in Microsoft Office; statistical knowledge 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. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
  
  

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

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

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

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  IT Services and IT Consulting

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