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Remote Clinical Trial Associate Jobs (NOW HIRING)

Braveheart Bio

Clinical Trial Manager

San Francisco, CA · On-site +1

$140K - $170K/yr

The Clinical Trial Manager (CTM) is a key member of the Clinical Operations team and will report ... This position is for remote work and may require domestic or international travel up to 25% (as ...

Civia Health

Clinical Trial Manager

Remote, US East Coast Job Type: Full-Time Reports To: Head of Country Delivery Internal Team Title: Clinical Trial Manager JOIN US AT CIVIA HEALTH Civia Health operates a nextgeneration SMO model ...

Absci

Senior Clinical Trial Manager

Vancouver, WA · On-site +1

$145K - $165K/yr

Senior Clinical Trial Manager Vancouver, WA (Onsite), Remote/Hybrid (US-based) We are seeking an experienced Senior Clinical Trial Manager to independently lead the end-to-end operational execution ...

IQVIA

Trial Delivery Manager, Multi TA

Boston, MA · Remote

Clinical Trial Management & Central Trial Oversight (FSP Model) Home Based Remote Role - East Coast Role Overview IQVIA is seeking an accomplished Senior Project Lead / Associate Director, Clinical ...

IQVIA

Trial Delivery Manager, Multi TA

Durham, NC · Remote

Clinical Trial Management & Central Trial Oversight (FSP Model) Home Based Remote Role - East Coast Role Overview IQVIA is seeking an accomplished Senior Project Lead / Associate Director, Clinical ...

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 ...

IQVIA

Trial Delivery Manager, Multi TA

Wayne, PA · Remote

Clinical Trial Management & Central Trial Oversight (FSP Model) Home Based Remote Role - East Coast Role Overview IQVIA is seeking an accomplished Senior Project Lead / Associate Director, Clinical ...

IQVIA

Trial Delivery Manager, Multi TA

Parsippany, NJ · Remote

Clinical Trial Management & Central Trial Oversight (FSP Model) Home Based Remote Role - East Coast Role Overview IQVIA is seeking an accomplished Senior Project Lead / Associate Director, Clinical ...

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 ...

Fortrea

Remote US or Canadian based. We are seeking candidates with either CAR T or Ophthalmology experience. Job Overview: The Clinical Trial Manager has ownership in the clinical delivery and operational ...

ICON

Clinical Trial Assistance

Blue Bell, PA · On-site +1

$32 - $43.75/hr

Clinical 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 ...

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 ...

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All JobsRemote Clinical Trial Associate Jobs

Remote Clinical Trial Associate information

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$70

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

As of Jul 6, 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.
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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 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.

GM/CEO, Clinical Trial Abundance Initiative

EQL Tech

San Francisco, CA • Remote

Full-time

Medical, PTO

Posted 23 hours 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