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Remote Icon Clinical Research Jobs in Raleigh, NC

Senior Project Manager, COA

Raleigh, NC ยท Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Project Manager, COA-ICON- US Remote (East Coast) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings ... Conduct on-site and remote visits/contacts, including Qualification, Initiation, Monitoring ...

New

Clinical Trial Manager

Raleigh, NC ยท On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

Cloud Engineer II

Raleigh, NC ยท Remote

$54.25 - $72.50/hr

Cloud Engineer II (US-based, ET/CT time zones only), Full time, Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

New

Job Posting Title- Director, Remote Research Clinician/Decentralised Clinical Trials Location: Home ... Drive advancement of technology-enabled clinical trial solutions, including workflow automation ...

Job Posting Title- Director, Remote Research Clinician/Decentralised Clinical Trials Location: Home ... Drive advancement of technology-enabled clinical trial solutions, including workflow automation ...

Showing results 21-40

Remote Icon Clinical Research information

See Raleigh, NC salary details

$18

$29

$41

How much do remote icon clinical research jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for remote icon clinical research in Raleigh, NC is $29.31, according to ZipRecruiter salary data. Most workers in this role earn between $25.00 and $31.06 per hour, depending on experience, location, and employer.

How does working remotely as a clinical research associate at ICON impact collaboration with on-site teams and study sites?

As a remote Clinical Research Associate (CRA) at ICON, you'll frequently collaborate with on-site teams and study sites using digital communication tools such as video conferencing, email, and specialized clinical trial management systems. While you may not be physically present at every site, you are still responsible for maintaining strong relationships, ensuring protocol compliance, and supporting site staff remotely. Regular virtual meetings and occasional on-site visits help bridge the distance, but self-motivation and proactive communication are essential for success in this remote setting. This structure offers flexibility but also requires strong organizational skills to manage multiple studies and maintain high-quality oversight.

What skills and qualifications are needed to thrive as a remote clinical research associate at ICON?

To thrive as a Remote Clinical Research Associate at ICON, you need a solid background in life sciences or healthcare, clinical trial experience, and often a relevant bachelor's degree or higher. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and knowledge of GCP/ICH guidelines are typically required, and certifications like ACRP or SOCRA are advantageous. Strong attention to detail, organizational skills, and effective communication are vital for managing remote site monitoring and collaborating with diverse teams. These skills ensure compliance, data accuracy, and seamless coordination across global clinical research projects.

What is the difference between Remote Icon Clinical Research vs Remote Clinical Data Coordinator?

AspectRemote Icon Clinical ResearchRemote Clinical Data Coordinator
CredentialsTypically requires life sciences degree, clinical research certificationsOften requires health or data management certifications, degree in health sciences
Work EnvironmentRemote, research sites, hospitals, or labsPrimarily remote, data entry and management systems
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch organizations, hospitals, clinical trial sponsors
Search & Comparison IntentUnderstanding clinical research roles, remote research jobsData management in clinical trials, remote data entry jobs

Remote Icon Clinical Research focuses on overseeing and managing clinical trials, often requiring scientific credentials and working in research environments. Remote Clinical Data Coordinators handle data entry and management tasks within clinical trials, primarily working remotely with a focus on data accuracy. Both roles are essential in clinical research but differ in responsibilities and required qualifications.

What is a remote Icon clinical research associate?

A Remote Icon Clinical Research job refers to a position within ICON plc, a global clinical research organization, where employees work remotely to support the design, execution, and management of clinical trials. These roles can include clinical research associates, project managers, data managers, and other professionals who help bring new medical treatments and drugs to market. Remote positions allow employees to work from home or another location outside of a traditional office, using digital tools to collaborate with teams and clients. This flexibility helps balance work-life needs while still contributing to important medical research. ICON is known for its focus on innovation and supporting remote work arrangements in the clinical research field.

What are the most commonly searched types of Icon Clinical Research jobs in Raleigh, NC?

The most popular types of Icon Clinical Research jobs in Raleigh, NC are:

What are popular job titles related to Remote Icon Clinical Research jobs in Raleigh, NC?

For Remote Icon Clinical Research jobs in Raleigh, NC, the most frequently searched job titles are:

What cities near Raleigh, NC are hiring for Remote Icon Clinical Research jobs?

Cities near Raleigh, NC with the most Remote Icon Clinical Research job openings:

Infographic showing various Remote Icon Clinical Research job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $60,975 per year, or $29.3 per hour.

Senior Project Manager, COA

Icon plc

Raleigh, NC โ€ข Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 7 days ago


Job description

Senior Project Manager, COA-ICON- US Remote (East Coast)

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.


Title: Senior Project Manager, COA

Location: Remote - USA (East Coast)

What you will do: As a Senior Project Manager within Patient Centered Solutions and Language Services at ICON, you will lead the delivery of clinical outcome assessment localization and electronic Clinical Outcome Assessment programs across multiple clinical studies. Serving as an embedded extension of a key pharmaceutical client's team, you will manage projects from initial intake through final delivery. You will coordinate cross-functional stakeholders, multilingual content, copyright and licensing activities, eCOA migrations, quality reviews, and project documentation. You will also help improve operational processes, reduce delivery timelines, and support the evaluation of new automation technologies.

Key responsibilities include:

  • Serve as the primary operational contact for incoming localization and eCOA requests, coordinating project kickoffs with study teams and other stakeholders.
  • Develop and manage project plans, requirements, timelines, deliverables, risks, and resource needs across multiple concurrent global and local studies.
  • Lead cross-functional collaboration among client stakeholders, study teams, localization specialists, technology teams, copyright holders, vendors, and other internal and external partners.
  • Assess the availability and readiness of questionnaires, translations, licenses, and supporting assets before translation and eCOA migration activities begin.
  • Coordinate copyright licensing, source-content review, translation preparation, multilingual deliverables, content modifications, and version-management activities.
  • Oversee automation-enabled eCOA questionnaire migrations and evaluate outputs for linguistic, formatting, technical, and content-readiness issues.
  • Identify and document migration defects, support root-cause analysis, recommend corrective actions, and provide structured feedback to technology teams.
  • Monitor project quality, timelines, review cycles, productivity, and stakeholder satisfaction through dashboards and status reporting.
  • Maintain complete, accurate, version-controlled, and audit-ready project documentation within approved SharePoint and document-management systems.
  • Identify opportunities to reduce bottlenecks, improve content reuse, shorten migration timelines, reduce manual effort, and standardize processes.
  • Support the validation and implementation of automation, artificial intelligence, and other emerging technologies used in localization and eCOA delivery.
  • Provide project leadership and guidance to cross-functional contributors while promoting quality, collaboration, and continuous improvement.

Your Profile:

  • Bachelor's degree in Life Sciences, Languages, Translation, Clinical Research, Healthcare Administration, Project Management, or a related discipline.
  • At least five years of relevant experience in clinical localization, clinical operations, clinical technology, or project management within a pharmaceutical, biotechnology, CRO, or related environment.
  • Demonstrated experience managing multiple concurrent projects, timelines, risks, deliverables, and cross-functional stakeholders in a fast-paced, matrix environment.
  • Strong understanding of multilingual content development, translation, and localization workflows.
  • Excellent communication, stakeholder-management, organizational, analytical, and problem-solving skills, with strong attention to detail.
  • Experience using SharePoint, document-management systems, collaboration platforms, and project-tracking tools.
  • Ability to work independently, manage competing priorities, and maintain complete, accurate, and audit-ready project documentation.
  • Direct experience with Clinical Outcome Assessments, electronic Clinical Outcome Assessments, and questionnaire migration projects is highly preferred.
  • Experience with copyright licensing, content acquisition, translation preparation, and version-management processes is highly preferred.
  • Familiarity with eCOA platforms, localization technologies, translation-management systems, or comparable clinical technologies is preferred.
  • Experience reviewing migration outputs, documenting defects, performing root-cause analysis, or supporting quality-validation activities is preferred.
  • Experience supporting automation, artificial intelligence, or clinical-technology pilot programs is preferred.
  • PMP or an equivalent project-management certification is preferred.

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 requesthere.

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