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Remote Clinical Trial Associate Jobs (NOW HIRING)

ICON

Senior Clinical Trial Manager

Senior Clinical Trial Manager ICON is a global healthcare intelligence and clinical research ... Train and mentor Clinical Research Associates (CRAs) to optimize their performance. * Timely Study ...

Jj

Senior Clinical Trial Leader

Raritan, NJ · On-site +1

Clinical Trial Project Management Job Category: Professional All Job Posting Locations ... Raritan, New Jersey, United States of America Remote work options may be considered on a case-by ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

Summary The Senior Clinical Trial Manager will lead the day-to-day activities in a clinical trial ... Perform clinical research site activities, which can include onsite or remote monitoring, co ...

ICON

Senior Clinical Trial Manager

Blue Bell, PA · On-site +1

As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities ... Train and mentor Clinical Research Associates (CRAs) to optimize their performance. * Timely Study ...

ICON

Senior Clinical Trial Manager

Blue Bell, PA · On-site +1

As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities ... Train and mentor Clinical Research Associates (CRAs) to optimize their performance. * Timely Study ...

ICON

Senior Clinical Trial Manager

Blue Bell, PA · On-site +1

As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities ... Train and mentor Clinical Research Associates (CRAs) to optimize their performance. * Timely Study ...

Natera

Senior Clinical Trial Manager

San Carlos, CA · On-site +1

$131K - $164K/yr

The Clinical Trial Manager should have experience in managing all aspects of the trials ... Remote USA $131,900--$164,900 USD OUR OPPORTUNITY Natera™ is a global leader in cell-free DNA ...

New

Argenx

Clinical Operations Development Lead

... Trial Associate(s) (CTAs). ROLES AND RESPONSIBILITIES * Provides strategic input and is accountable for all clinical related aspects within the assigned therapeutic indication/program and in line ...

Character Biosciences

Senior Clinical Trial Manager

$153K - $180K/yr

Remote The Opportunity : Character Biosciences is seeking a Senior Clinical Trial Manager who will be responsible for leading all aspects of clinical trial management from study-start up through ...

Emmes

In-House CRA II

Rockville, MD · Remote

Overview In-House CRA II US Remote Emmes Group: Building a better future for us all. Emmes Group is ... The In-House CRA II may also be referred to as a Clinical Trial Associate on some contracts.

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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 Jun 13, 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.

Which is better, CRA or CRC?

A Clinical Research Associate (CRA) typically oversees multiple clinical trials, monitors site compliance, and ensures data quality, often working remotely or traveling to sites. A Clinical Research Coordinator (CRC) manages daily trial activities at a specific site, handles patient interactions, and maintains study documentation. Both roles are essential, with CRAs focusing on oversight and CRCs on site management; the choice depends on preferred work environment and career goals.

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.

Is CRA an entry-level job?

A Clinical Trial Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, understanding of Good Clinical Practice (GCP), and sometimes relevant certifications. Entry-level roles in clinical research may include Clinical Research Coordinator or Clinical Research Assistant, with CRAs often advancing from these positions after gaining experience. However, some companies offer junior or trainee CRA roles for candidates with limited experience who demonstrate strong organizational and communication skills.

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.

Is a clinical trial associate a good career?

A clinical trial associate is a valuable role in the healthcare and pharmaceutical industries, responsible for coordinating and monitoring clinical trials to ensure compliance and data integrity. It offers opportunities for career growth, requires attention to detail, and often involves working with specialized software and regulatory guidelines. The role can be stable and rewarding for those interested in medical research and patient safety.

Can a clinical research associate work remotely?

Yes, many clinical research associates (CRAs) can work remotely, especially with the increased use of electronic data capture and remote monitoring tools. Remote work allows CRAs to oversee trial sites, review data, and communicate with teams virtually, though some in-person site visits may still be required depending on the study and employer policies.
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Remote Clinical Trial Associate jobs near you
Infographic showing various Remote Clinical Trial Associate job openings in the United States as of June 2026, with employment types broken down into 7% Full Time, and 93% Part Time. Highlights an 70% Physical, 6% Hybrid, and 24% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

GM/CEO, Clinical Trial Abundance Initiative

EQL Tech

San Francisco, CA • Remote

Full-time

Medical, PTO

Posted 8 days ago

Job description

General Manager/CEO, Clinical Trial Abundance Initiative

Location: Remote (US-Based) | Type: Full-Time | Reports to: CEO, philanthropic foundation

EQL Tech is partnering with two philanthropic foundations collaborating to reshape the clinical trial landscape to ensure that groundbreaking therapies reach patients swiftly and equitably. The foundation aims to overcome systemic barriers that limit trial access and diversity, with a goal to improve the representativeness of clinical trial populations and maximize the impact of innovative solutions in health.

Role Overview

The foundation is seeking a General Manager/CEO for its nascent Clinical Trial Abundance Initiative. In this role, you will lead a transformative effort to decentralize clinical trial access, promoting a model that prioritizes patient-centered care and ensures diverse participation. You will develop and execute strategies that empower health systems, community organizations, and patients to engage more fully in the clinical trial process.

Key Responsibilities
  • Design and implement strategies to increase clinical trial accessibility, particularly for underrepresented populations.
  • Collaborate with health systems, patient advocacy groups, and research institutions to streamline participation pathways and share effective outreach practices.
  • Facilitate the integration of community engagement and ecosystem building methodologies into clinical trial planning and execution, ensuring trials reflect real-world patient diversity.
  • Advocate for policy changes at local, state, and federal levels to enhance regulatory flexibility in clinical trial designs.
  • Monitor and evaluate initiative progress, iterating on strategies based on data-driven insights and stakeholder feedback.
  • Engage with thought leaders and subject matter experts to champion innovative practices that redefine the clinical trial framework.

Requirements

Who You Are
  • Experienced Leader: You have 5+ years of experience in health policy, research, or clinical operations, with a demonstrated track record in managing complex initiatives that produce meaningful outcomes.
  • Passionate Advocate: You are committed to equity in healthcare and have a deep understanding of the barriers that hinder patient participation in clinical trials.
  • Strategic Thinker: You possess a data-driven mindset and can develop innovative solutions to overcome systemic challenges.
  • Collaborative Partner: You thrive in collaborative environments, building relationships with stakeholders across diverse sectors to drive impactful change.
  • Excellent Communicator: You can articulate complex concepts clearly and persuasively, whether in writing or speaking, to engage and inform a wide range of audiences.
Qualifications
  • Master’s degree in a relevant field (public health, health administration, scientific research, etc.). PhD or equivalent professional experience is a plus.
  • Proven experience in clinical research, trial design, or healthcare innovation.
  • Strong understanding of regulatory frameworks governing clinical trials and the healthcare system.
  • Experience driving initiatives that promote health equity and patient engagement.
  • Willingness to travel (as required) to attend conferences, meetings, and stakeholder consultations.

Benefits

  • Competitve salary, commensurate with experience
  • Private Health Insurance
  • Paid Time Off
  • Work From Home
  • Training & Development