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New · posted Nov 1

ICON · Pharmaceuticals

Senior Clinical Trial Manager

  • Remote, US
  • Remote
  • Full-time
  • Manager
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EmploymentFull-time
LocationRemote, US
DeadlineOpen until filled

The role

Senior Clinical Trial Manager, United States, Remote

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.

What you need

You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

  • A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization.
  • Bachelor's degree in health, life sciences, or other relevant fields of study.
  • At least 10+ years of relevant experience in clinical trial management.
  • Preferred: 2+ years of monitoring experience.
  • Experience in managing complex or global trials is advantageous.
  • Preferred: Experience in managing all trial components from start-up to database lock.
  • Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.
  • Willingness to travel as required (approximately 25%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

What you'll do

Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability.

Key responsibilities include:

  • Budget Oversight Oversee the clinical portion of the budget to ensure efficient resource allocation.
  • Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight.
  • Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance.
  • Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.
  • Improving Study Integrity Review trip reports and implement corrective and preventative action plans when necessary.Building Productive Relationships: Foster productive relationships with Sponsors, vendors, and cross-functional teams.

Pay and benefits

ICON didn't publish pay for this role

See what similar roles pay on Regulatory Jobs, or try the salary calculator.

Rewards & Benefits

  • Competitive base salary and performance related incentives

  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable

  • Retirement and pension plans

  • Life assurance and disability coverage

  • Employee assistance programmes and wellbeing resources

  • Learning and development opportunities through structured training and career pathways

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Equal opportunity, accessibility and legal noticesICON's statements, word for word

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

Job intelligence

The context around this role

Live data · November 1, 2026

Salary intelligence

How the pay compares

Manager roles in the US44 roles publishing pay

Middle half $150,125 to $175,000, median $163,000
Annual base pay
Annual base payLowMedianHigh
All US$150,125$163,000$175,000

Comparisons: the base pay employers published on open Clinical Trial Management roles at the same level on Regulatory Jobs, November 1, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Trial Management

The general path across 69 open Clinical Trial Management roles on Regulatory Jobs, with the titles they carry most. Not ICON's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: Clinical Trial Assistant · Clinical Study Specialist

    $87K median7 open
  2. One step back

    Senior & Principal

    Often: Regional Clinical Trial Management Senior Associate · Clinical Research Leader

    $131K median6 open
  3. This role

    Manager

    Often: Senior Clinical Trial Manager · Clinical Trial Manager

    $163K median55 open
  4. Next step

    Director

    Often: Associate Director, Clinical Development Trial Lead

Skills DNA

What this role leans on

How many of the posting's 20 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

Documentation and SOPs: 1 lineQuality systems and risk: 1 lineClinical trial conduct: 9 linesCollaboration and leadership: 8 linesDocumentationQuality systemsClinical trialsTeamwork
  • Clinical trial conduct9
  • Collaboration and leadership8
  • Documentation and SOPs1
  • Quality systems and risk1

Company hiring pulse

ICON on Regulatory Jobs

106
Open roles
56
Distinct roles
30
Locations

By discipline

  • Clinical96 91%
  • Quality7 7%
  • Regulatory3 3%

By level

  • Senior & Principal45 42%
  • Associate & Specialist43 41%
  • Manager15 14%
See all 106 ICON roles

More roles at ICON

All 106 ICON roles

Similar Clinical Trial Management roles elsewhere

Senior Clinical Trial Manager at ICON

Open until filled.

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