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Work From Home Clinical Trial Assistant Jobs (NOW HIRING)

$35.50 - $48.25/hr

From our global network of research and development sites, we are committed to discovering and ... Assist with the planning, start-up, execution, and close-out of clinical trials, including ...

Clinical Trial Manager

Waltham, MA · On-site +1

$140K - $200K/yr

... who is looking to work in a fast paced, growth mindset organization focused on developing ... * Assist in managing CRO and other study vendors day-to-day activities working directly with the ...

Founded in 2018, Character has raised capital from leading investors at the intersection of health ... Your work translates directly into Character's mission: the studies you run generate the clinical ...

Clinical Trial Associate

Redwood City, CA · On-site +1

$41 - $56/hr

Remote (Bay Area preferred) Primary Responsibilities: * Assist study teams with the collection ... Work is generally performed in an office, laboratory, clinical site or remote home office ...

Position Summary The Clinical Trial Navigator (CTN) is a Registered Nurse who serves as a key ... Remote based position: must have a private, secure office to work from * Travel Requirement ...

Clinical Trial Associate

Redwood City, CA · On-site +1

$60K - $91K/yr

Remote (Bay Area preferred) Primary Responsibilities: * Assist study teams with the collection ... Work is generally performed in an office, laboratory, clinical site or remote home office ...

Home-based in the U.S. Responsibilities & Key Tasks Lead global, cross-functional trial teams to ... Excellent interpersonal and communication skills, with the ability to work across geographies and ...

Work closely with study investigators, site staff, and sponsor/CRO teams to support highquality trial execution * Adhere to Good Clinical Practice (GCP), SOPs, and ethical guidelines at all times

Work closely with study investigators, site staff, and sponsor/CRO teams to support highquality trial execution * Adhere to Good Clinical Practice (GCP), SOPs, and ethical guidelines at all times

Our office-based work policy encourages a dynamic work environment, prescribing a minimum of 2 days ... Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for ...

Showing results 21-40

Work From Home Clinical Trial Assistant information

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How much do work from home clinical trial assistant jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for work from home clinical trial assistant in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What is a work from home clinical trial assistant?

A Work From Home Clinical Trial Assistant is a professional who supports the administrative and operational aspects of clinical trials while working remotely. Their responsibilities may include managing trial documentation, scheduling meetings, maintaining databases, and communicating with study sites and team members. This role helps ensure that clinical studies are conducted efficiently and in compliance with regulatory standards, all from a home office setting. Strong organizational skills, attention to detail, and proficiency with digital tools are essential for success in this position.

What are the key skills and qualifications needed to thrive as a work from home clinical trial assistant?

To thrive as a Work From Home Clinical Trial Assistant, you need a strong understanding of clinical research processes, attention to detail, and a relevant degree such as life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) software, and regulatory documentation tools is typically required. Excellent organization, time management, and communication skills are essential for collaborating remotely and ensuring compliance. These abilities are crucial for maintaining trial integrity, meeting deadlines, and supporting successful clinical study outcomes.

What are some common challenges faced by work from home clinical trial assistants, and how can they be addressed?

Work From Home Clinical Trial Assistants often face challenges such as coordinating communication across distributed teams and managing multiple tasks remotely. Staying organized with digital tools and maintaining proactive communication with study coordinators, investigators, and other stakeholders is essential. Regular virtual meetings and clear documentation help ensure that deadlines are met and trial data is accurately maintained. Embracing collaborative platforms and setting a structured daily routine can significantly improve efficiency and reduce the feeling of isolation.
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What cities are hiring for Work From Home Clinical Trial Assistant jobs?

Cities with the most Work From Home Clinical Trial Assistant job openings:

What states have the most Work From Home Clinical Trial Assistant jobs?

States with the most job openings for Work From Home Clinical Trial Assistant jobs include:

Infographic showing various Work From Home Clinical Trial Assistant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, and 3% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Associate Clinical Trial Manager - PhD / Post-Doc Experience - Dallas, TX

Medpace, Inc.

Dallas, TX • On-site, Remote

$33.25 - $45.25/hr

Full-time

Medical, Retirement, PTO

Re-posted 7 days ago


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

16th of 75 rated research


Job description

Job Summary

Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in our Dallas office.  The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities.  Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.

This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

Responsibilities
  • Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager;
  • Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy;
  • Compile and maintain project-specific status reports within the clinical trial management system;
  • Interact with the internal project team, Sponsor, study sites, and third-party vendors;
  • Provide oversight and quality control of our internal regulatory filing system;
  • Provide oversight and management of study supplies;
  • Create and maintain project timelines; and
  • Coordinate project meetings and produce quality minutes.
Qualifications
  • PhD in Life Sciences;
  • Fluency in English with solid presentation skills;
  • Ability to work in a fast-paced dynamic industry within an international team; 
  • Prior experience within the CRO or pharmaceutical industry not required but will be advantageous; and
  • Excellent computer (word-processing, databases, Excel, Windows), organisational, and communication skills.
Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events 

Please note benefits may vary based on country. 

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Employment Type: OTHER

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992