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Remote Clinical Trial Manager Jobs in Raleigh, NC

ICON

Clinical Trial Manager

Raleigh, NC · On-site +1

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

Allucent

Clinical Trial Lead

Cary, NC · Remote

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research ...

IQVIA

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 ...

IQVIA

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 ...

IQVIA

Clinical Project Lead, Oncology

Durham, NC · Remote

$68K - $232K/yr

In this remote role you will serve as the primary country-level leader for clinical trial delivery ... Lead end-to-end country-level trial management , from study start-up through database lock and ...

IQVIA

Clinical Project Lead, Oncology

Durham, NC · Remote

$68K - $232K/yr

In this remote role you will serve as the primary country-level leader for clinical trial delivery ... Lead end-to-end country-level trial management , from study start-up through database lock and ...

Icon plc

Senior Clinical Research Associate

Cary, NC · Remote

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

Icon plc

Senior Clinical Research Associate

Raleigh, NC · Remote

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

Icon plc

Senior Clinical Research Associate

Raleigh, NC · Remote

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

Bruno

Clinical Payments Specialist

Raleigh, NC · Remote

Remote (United States) Employment Type: Full-Time Our client is seeking a Budget Operations Specialist to support global clinical trial operations by managing investigator budgets, site setup, and ...

Bruno

Clinical Payments Specialist

Raleigh, NC · On-site +1

Remote (United States) Employment Type: Full-Time Our client is seeking a Budget Operations Specialist to support global clinical trial operations by managing investigator budgets, site setup, and ...

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All JobsClinical Trial JobsRemote Clinical Trial Manager JobsRemote Clinical Trial Manager Jobs in Raleigh, NC

Remote Clinical Trial Manager information

See Raleigh, NC salary details

$28

$60

$93

How much do remote clinical trial manager jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for remote clinical trial manager in Raleigh, NC is $60.77, according to ZipRecruiter salary data. Most workers in this role earn between $49.33 and $68.46 per hour, depending on experience, location, and employer.

What is the difference between Remote Clinical Trial Manager vs Remote Clinical Research Associate?

AspectRemote Clinical Trial ManagerRemote Clinical Research Associate
CredentialsTypically requires a Bachelor's or higher in life sciences, with experience in trial managementUsually holds a Bachelor's in life sciences or related field, with certification in clinical research (e.g., CCRP)
Work EnvironmentOversees multiple sites, manages trial timelines, budgets, and teams remotelyMonitors trial sites, ensures protocol compliance, and collects data remotely
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical research organizations

The Remote Clinical Trial Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Remote Clinical Research Associate primarily monitors trial sites and data collection. Both roles require clinical research knowledge and often work remotely within the same industry sectors.

What does a remote clinical trial manager do?

Remote clinical trial managers monitor the process of clinical testing from home or another location outside of the office or lab. In this role, you may collaborate with the clinical project manager to create outlines for the trial, research relevant information from existing medical studies, and help ensure the scope of the testing is enough to move the product forward to the next phase. Products may include pharmaceuticals, medical devices, or other forms of medical treatments. Your job duties also involve creating strategies for efficient testing methods, checking that all tests comply with safety standards and current government regulations, documenting results, and supervising research assistants.

What are the key skills and qualifications needed to thrive as a remote clinical trial manager, and why are they important?

To thrive as a Remote Clinical Trial Manager, you need expertise in clinical research, regulatory compliance, and project management, usually supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and GCP certification are typically required. Exceptional organizational skills, proactive communication, and the ability to lead cross-functional teams remotely set top performers apart. These competencies are crucial for ensuring trial integrity, regulatory adherence, and seamless coordination across distributed teams.

How does a remote clinical trial manager typically collaborate with on-site study teams and stakeholders?

As a Remote Clinical Trial Manager, you will frequently coordinate with on-site study teams, investigators, and sponsors through virtual meetings, project management platforms, and regular reporting. Effective communication and proactive problem-solving are essential for ensuring trial milestones are met and regulatory requirements are followed, despite not being physically present. You may also oversee remote monitoring visits, address site queries, and facilitate cross-functional collaboration between data management, safety, and regulatory teams. This structure allows for flexibility while maintaining strong oversight and quality standards.

What is a remote clinical trial manager?

A Remote Clinical Trial Manager is a professional responsible for overseeing the planning, execution, and management of clinical trials from a remote location. They coordinate with various teams, ensure regulatory compliance, monitor trial progress, and manage budgets and timelines, all while working off-site. This role typically involves using digital tools to communicate, track data, and ensure the trial runs smoothly and efficiently. Remote Clinical Trial Managers are essential in facilitating clinical research, especially in decentralized or multi-site studies. They play a key role in ensuring that clinical trials meet both scientific and regulatory standards.
More about Remote Clinical Trial Manager jobs
What are the most commonly searched types of Remote Clinical Trial jobs in Raleigh, NC? The most popular types of Remote Clinical Trial jobs in Raleigh, NC are:
What are popular job titles related to Remote Clinical Trial Manager jobs in Raleigh, NC? For Remote Clinical Trial Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Remote Clinical Trial Manager jobs in Raleigh, NC look for? The top searched job categories for Remote Clinical Trial Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Remote Clinical Trial Manager jobs? Cities near Raleigh, NC with the most Remote Clinical Trial Manager job openings:
Remote Clinical Trial Manager jobs near you
Infographic showing various Remote Clinical Trial Manager job openings in Raleigh, NC as of August 2026, with employment types broken down into 90% Full Time, 5% Part Time, and 5% Contract. Highlights an 100% Remote job distribution, with an average salary of $126,404 per year, or $60.8 per hour.

Clinical Trial Manager

ICON

Raleigh, NC • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 4 days ago

Job description

Clinical Trial Manager - Phase I oncology
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.
What you will be doing
  • Manage the day-to-day operations of assigned trials and responsibilities to ensure completion per established project team goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements
  • Leads or supports cross-functional trial teams, including vendors
  • Ensures accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders
  • Proactively identify and resolve issues that arise during trial conduct; manage escalation of trial-related issues
  • Participate in or lead the development of core trial documents, trial plans and system set-up; participate in preparation and ensure operational excellence of protocol and implementation of appropriate systems, standards, and processes to ensure quality across investigative sites, vendors, and data
  • Participate in or lead preparation of vendor requirements and project scope and selection of trial vendors; effectively manage interactions and escalations with vendor trial team
  • Participate in or lead feasibility assessment and selection of countries and sites for trial conduct
  • Participate in or facilitates site engagement and communications with investigators and/or staff to support trial milestones and deliverables
  • Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top line results; participate in data reviews and review of statistical analysis plans
  • Participate in or lead set-up and implementation of effective investigator and site monitor training; coordinate operational and therapeutic area training for internal and external trial team members
  • Provide oversight and direction to trial team members for trial deliverables
  • Manage clinical trial budget and associated vendor contracts, including tracking and data in associated systems
  • Ensure quality and completeness of TMF for assigned clinical trials
  • Participates in inspection readiness activities including coordination of clinical trial team deliverables
  • Participate in the evaluation and implementation of patient-focused strategies for assigned trials, as applicable
  • Responsible for the management of budgets, timelines and resources for assigned clinical trial responsibilities

Your profile
  • BA/BS degree with at least 3 years clinical trial experience or advanced degree (MS/PhD/PharmD) with at least 2 years clinical trial management experience
  • Must have strong knowledge of ICH/GCP guidelines and regulatory requirements
  • Must have knowledge of protocol and clinical drug development processes, clinical trial design, trial planning and management, and monitoring
  • Requires project management skills and trial leadership ability
  • Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability
  • Fluent in English
  • Experience in Phase I oncology
  • Global experience with primary focus on independent vendor set up and management, oncology cohort management and experience in supporting dose escalation safety meetings.
  • May be asked to Work East coast hours if located further West
  • Moderate (~25%) travel required

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

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