Senior Clinical Trial Manager
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Before you apply
LocationUS, Blue Bell (ICON); US, Raleigh, NC
Work modeon-site
Typefull-time
SenioritySenior
Experience10+ yrs
Company size10,000+ people
PostedOct 22, 2026 · 1w ago
Verified live1d ago
At a glanceSummarised by Seekless from the posting.
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.
Willingness to travel as required (approximately 25%)
2+ years of monitoring experience.
Experience in managing complex or global trials is advantageous.
Experience in managing all trial components from start-up to database lock.
Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Benefits
Health insurance
Dental coverage
Vision coverage
Retirement plan
Life assurance
Disability coverage
Employee assistance program
Learning and development
Bonus
About the role
Senior Clinical Trial Manager, United States, Remote
About the company
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 Will 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.
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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.
Your Profile:
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%)
Legal
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
•
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
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
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