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Remote Clinical Trial Associate Jobs (NOW HIRING)

Clinical Trial Associate

Blue Bell, PA ยท On-site +1

$32 - $43.75/hr

Clinical Trial Associate 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 ...

Clinical Trial Associate

Blue Bell, PA ยท On-site +1

$32 - $43.75/hr

Clinical Trial Associate 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 ...

Minimum of 4 years of clinical trial management and 2+ years clinical research associate with on-site/remote clinical monitoring experience in the biotechnology/pharmaceutical/CRO industry * Robust ...

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ...

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ...

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ...

Clinical Trial Manager

$130K - $150K/yr

Role Overview: We are seeking a Clinical Trial Manager (CTM) to support our U.S. Clinical ... Associate Director, Team Lead Site Operations Location : Fully Remote Salary Range: $130,000 - $150 ...

Senior Clinical Trial Manager

New York, NY ยท Remote

$149K - $200K/yr

... or Associate Director/Director of Clinical Operations. In this role, you will: * Support the ... This position is open to both remote and hybrid models. The hybrid position would be office-based ...

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... Support the operational strategy related to assigned vendors, data flow, drug supply, remote ...

Clinical Trial Manager

San Francisco, CA ยท On-site +1

$145K - $165K/yr

About the Job We are hiring a Clinical Trial Manager to support the successful execution of our ... as a remote work day * Ability to travel as needed (10% - 15%) * Qualified candidates must be ...

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Remote Clinical Trial Associate information

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

As of Jul 5, 2026, the average hourly pay for remote clinical trial associate in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What does a Remote Clinical Trial Associate do?

A Remote Clinical Trial Associate (CTA) supports the planning, execution, and management of clinical trials from a remote location. Their responsibilities include handling documentation, assisting with regulatory submissions, maintaining trial records, and coordinating communication between trial sites, sponsors, and regulatory bodies. Remote CTAs play a crucial role in ensuring that trials are conducted according to protocols, timelines, and regulatory requirements, all while working offsite. This allows for greater flexibility and can improve efficiency in clinical research processes.

What are the key skills and qualifications needed to thrive as a Remote Clinical Trial Associate, and why are they important?

To thrive as a Remote Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines, and typically a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and Good Clinical Practice (GCP) certification are commonly required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for managing study documentation and collaborating with remote teams. These competencies ensure trials are conducted efficiently, compliantly, and with high data integrity in a virtual environment.

What are some common challenges faced by Remote Clinical Trial Associates, and how can they be managed?

Remote Clinical Trial Associates often encounter challenges such as maintaining consistent communication with on-site teams, managing multiple studies across different time zones, and ensuring accurate documentation while working virtually. These can be managed by leveraging robust digital communication tools, setting clear expectations for updates, and staying organized with project management software. Proactively building relationships with colleagues and participating in regular virtual meetings also helps ensure alignment and smooth coordination throughout the trial process.
More about Remote Clinical Trial Associate jobs
What cities are hiring for Remote Clinical Trial Associate jobs? Cities with the most Remote Clinical Trial Associate job openings:
What are the most commonly searched types of Remote Clinical Trial jobs? The most popular types of Remote Clinical Trial jobs are:
What states have the most Remote Clinical Trial Associate jobs? States with the most job openings for Remote Clinical Trial Associate jobs include:
Infographic showing various Remote Clinical Trial Associate job openings in the United States as of June 2026, with employment types broken down into 76% Full Time, and 24% Part Time. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.
Clinical Trial Associate

Clinical Trial Associate

ICON

Blue Bell, PA โ€ข On-site, Remote

$32 - $43.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 3 days ago


Job description

Clinical Trial Associate
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 Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
  • Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
  • Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
  • Support the preparation of study-related materials, such as informed consent forms and case report forms.
  • Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
  • Contribute to the tracking and reporting of clinical trial metrics and milestones.

Your Profile:
You will bring relevant clinical research experience, along with the following qualifications and skills.
Required qualifications and experience:
  • Bachelor's degree in a scientific or healthcare-related field.
  • Prior experience or strong interest in clinical research.
  • Knowledge of clinical trial processes, regulations, and guidelines.
  • Excellent organizational and communication skills.
  • Ability to work collaboratively in a fast-paced environment with attention to detail.
  • Willingness to travel as required (approximately 10%)

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