Country Lead Monitor
Raleigh, NC · On-site
As a 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 ...
Country Lead Monitor
Raleigh, NC · On-site
As a 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 ...
As a 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 ...
Quick apply
As a 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 ...
Country Lead Monitor
Raleigh, NC · On-site
As a 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 ...
Country Lead Monitor
Raleigh, NC · On-site
As a 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 ...
As a 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 ...
As a 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 ...
Country Lead Monitor
Raleigh, NC · On-site
As a 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 ...
Country Lead Monitor
Raleigh, NC · On-site
As a 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 ...
As a 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 ...
As a 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 ...
Senior Global Trial Manager
Durham, NC · On-site +1
$93K - $232K/yr
As a Global Trial Manager, you will play a crucial role in clinical trial delivery, leading ... Ensuring clinical delivery of assigned projects in compliance with regulatory requirements ...
Senior Global Trial Manager
Durham, NC · On-site +1
$93K - $232K/yr
As a Global Trial Manager, you will play a crucial role in clinical trial delivery, leading ... Ensuring clinical delivery of assigned projects in compliance with regulatory requirements ...
Senior Global Trial Manager
Durham, NC · On-site +1
$93K - $232K/yr
As a Global Trial Manager, you will play a crucial role in clinical trial delivery, leading ... Ensuring clinical delivery of assigned projects in compliance with regulatory requirements ...
Senior Global Trial Manager
Durham, NC · On-site +1
$93K - $232K/yr
As a Global Trial Manager, you will play a crucial role in clinical trial delivery, leading ... Ensuring clinical delivery of assigned projects in compliance with regulatory requirements ...
Country Lead Monitor
Raleigh, NC · On-site
As a 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 ...
Country Lead Monitor
Raleigh, NC · On-site
As a 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 ...
Country Lead Monitor
Raleigh, NC · On-site
As a 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 ...
Country Lead Monitor
Raleigh, NC · On-site
As a 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 ...
Country Lead Monitor
Raleigh, NC · On-site
As a 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 ...
Country Lead Monitor
Raleigh, NC · On-site
As a 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 ...
As a 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 ...
Quick apply
As a 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 ...
As a 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 ...
Quick apply
As a 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 ...
Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level ... Strong experience managing CROs, vendors, and external partners. * Extensive knowledge of ICH-GCP ...
Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level ... Strong experience managing CROs, vendors, and external partners. * Extensive knowledge of ICH-GCP ...
Clinical Trials Manager- Remote
Chapel Hill, NC · Remote
$62 - $64.73/hr
Support development and maintenance of the Trial Master File (TMF) and ensure document quality and ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...
Quick apply
Clinical Trials Manager- Remote
Chapel Hill, NC · Remote
$62 - $64.73/hr
Support development and maintenance of the Trial Master File (TMF) and ensure document quality and ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...
... the close of trial. Conduct, drive, and manage country-specific feasibility and site pre ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...
... the close of trial. Conduct, drive, and manage country-specific feasibility and site pre ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...
Develop and manage study timelines, contract/budget negotiations, and risk mitigation plans to ... Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level.
Quick apply
Develop and manage study timelines, contract/budget negotiations, and risk mitigation plans to ... Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level.
Senior Clinical Project Manager
Raleigh, NC · On-site
$140 - $200/hr
Develop and manage study timelines, contract/budget negotiations, and risk mitigation plans to ... Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level.
New
Senior Clinical Project Manager
Raleigh, NC · On-site
$140 - $200/hr
Develop and manage study timelines, contract/budget negotiations, and risk mitigation plans to ... Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level.
New
Develop and manage study timelines, contract/budget negotiations, and risk mitigation plans to ... Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level.
Develop and manage study timelines, contract/budget negotiations, and risk mitigation plans to ... Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level.
Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings ... Clinical Trial Management System (CTMS) and Electronic Document Management System (EDMS); Site ...
Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings ... Clinical Trial Management System (CTMS) and Electronic Document Management System (EDMS); Site ...
Associate Clinical Trial Manager information
See Raleigh, NC salary details
$16.82 - $21.50
4% of jobs
$21.50 - $26.17
8% of jobs
$26.17 - $30.84
12% of jobs
$30.98 is the 25th percentile. Wages below this are outliers.
$30.84 - $35.52
26% of jobs
$35.52 - $40.19
18% of jobs
$41.81 is the 75th percentile. Wages above this are outliers.
$40.19 - $44.86
19% of jobs
$44.86 - $49.54
6% of jobs
$49.54 - $54.21
2% of jobs
$54.21 - $58.88
1% of jobs
$58.88 - $63.56
1% of jobs
$63.56 - $68.23
2% of jobs
$16
$38
$68
How much do associate clinical trial manager jobs pay per hour?
As of Aug 19, 2026, the average hourly pay for associate clinical trial manager in Raleigh, NC is $38.87, according to ZipRecruiter salary data. Most workers in this role earn between $31.30 and $42.74 per hour, depending on experience, location, and employer.
What does an associate clinical trial manager do?
An Associate Clinical Trial Manager assists in the planning, execution, and management of clinical trials to ensure they are conducted in accordance with regulatory guidelines and company protocols. They support the Clinical Trial Manager by coordinating study timelines, managing vendors and sites, and overseeing documentation and reporting. This role involves collaborating with cross-functional teams, identifying and resolving issues, and ensuring that trials meet quality and compliance standards. Associate Clinical Trial Managers play a key part in bringing new treatments to market efficiently and safely.
What are the key skills and qualifications needed to thrive as an associate clinical trial manager?
To thrive as an Associate Clinical Trial Manager, you need a solid understanding of clinical trial processes, regulatory guidelines, and a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as GCP (Good Clinical Practice) are typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for managing timelines and collaborating with multiple stakeholders. These skills and qualifications ensure clinical trials run smoothly, comply with regulations, and deliver reliable results.
What are some common challenges faced by associate clinical trial managers when coordinating cross-functional teams?
Associate Clinical Trial Managers often encounter challenges related to aligning objectives and communication among cross-functional teams, such as regulatory, clinical operations, data management, and vendors. Managing timelines, ensuring all parties are updated on protocol changes, and resolving conflicts between departments can be complex, especially in a fast-paced environment. Proactive communication, attention to detail, and strong organizational skills are essential for overcoming these challenges and maintaining trial quality and compliance.
What is the difference between Associate Clinical Trial Manager vs Clinical Trial Coordinator?
| Aspect | Associate Clinical Trial Manager | Clinical Trial Coordinator |
|---|---|---|
| Responsibilities | Oversees trial operations, manages teams, ensures compliance, and supports trial planning | Coordinates trial activities, manages documentation, schedules visits, and assists with data collection |
| Required Credentials | Bachelor's degree, experience in clinical trials, knowledge of GCP | Bachelor's degree, experience in clinical settings, familiarity with trial procedures |
| Work Environment | Typically in clinical research settings, working closely with managers and teams | Often in clinical sites or research offices, supporting trial staff |
The Associate Clinical Trial Manager and Clinical Trial Coordinator roles share similar educational backgrounds and work environments. However, the Associate Clinical Trial Manager has broader responsibilities, including overseeing trial operations and managing teams, while the Clinical Trial Coordinator focuses on day-to-day coordination and documentation tasks. Both roles are essential in clinical research, with the manager position having a higher level of oversight and strategic involvement.
How much does an Associate Clinical Trial Manager earn?
An Associate Clinical Trial Manager typically earns between $70,000 and $100,000 annually, depending on experience, location, and the size of the organization. Entry-level positions may start lower, while experienced managers with certifications can earn higher salaries. Compensation often includes benefits such as health insurance and performance bonuses.
How to become an Associate Clinical Trial Manager?
To become an Associate Clinical Trial Manager, candidates typically need a bachelor's degree in life sciences, healthcare, or a related field, along with experience in clinical research or project coordination. Gaining knowledge of Good Clinical Practice (GCP) guidelines and clinical trial management systems is beneficial. Some roles may require certification such as the Certified Clinical Research Professional (CCRP) or similar credentials.
What are the most commonly searched types of Clinical Trial Manager jobs in Raleigh, NC?
The most popular types of Clinical Trial Manager jobs in Raleigh, NC are:
What are popular job titles related to Associate Clinical Trial Manager jobs in Raleigh, NC?
For Associate Clinical Trial Manager jobs in Raleigh, NC, the most frequently searched job titles are:
- Decentralized Clinical Trials
- Part Time Clinical Trial
- Clinical Research Psychologist
- Clinical Research Monitor
- Clinical Research Psychiatrist
- Clinical Trial Specialist
- Clinical Trial Associate
- Senior Clinical Research Associate Oncology
- Internship Clinical Psychology Research Assistant
- Junior Clinical Trial Manager
What job categories do people searching Associate Clinical Trial Manager jobs in Raleigh, NC look for?
The top searched job categories for Associate Clinical Trial Manager jobs in Raleigh, NC are:
- Clinical Research Assistant
- Clinical Trial Management Associate
- Clinical Trials
- Full Time Clinical Research Associate
- Clinical Trial Data Entry
- Clinical Research Manager
- Entry Level Clinical Research Oncology
- Full Time Clinical Trials Test Subject
- Entry Level Clinical Study Startup
- Remote Merck Clinical Trials
What cities near Raleigh, NC are hiring for Associate Clinical Trial Manager jobs?
Cities near Raleigh, NC with the most Associate Clinical Trial Manager job openings:
Full-time
Medical, Dental, Vision, Life, Retirement
Posted 7 days ago
Job description
Country Lead Monitor
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 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:
You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes.
Key responsibilities include:
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:
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:
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
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 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:
You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes.
Key responsibilities include:
- Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
- Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
- Build and manage strong relationships with trial investigators and stakeholders.
- Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
- Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.
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:
- University degree in medicine, science, or equivalent combination of education & experience
- Demonstrated ability to drive the clinical deliverables of a study
- Subject matter expertise in the designated therapeutic area
- Prior monitoring experience is preferred
- 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.
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