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Remote Clinical Trial Part Time Jobs (NOW HIRING)

WellQor

Remote Clinical Therapist - Georgia

Woodstock, GA · Remote

$80K - $100K/yr

Your Role as a Remote Clinical Therapist: At WellQor, you'll help your clients overcome mental ... Some WellQor therapists work part time, and others carry full caseloads. Whatever your lifestyle ...

WellQor

Remote Clinical Therapist - CA

San Francisco, CA · Remote

$80K - $120K/yr

Some WellQor therapists work part time, and others carry full caseloads. Whatever your lifestyle demands, we're here to meet you where you're at. * Consult with your clinical director and your ...

WellQor

Remote Clinical Therapist - CA

Los Angeles, CA · Remote

$80K - $120K/yr

Some WellQor therapists work part time, and others carry full caseloads. Whatever your lifestyle demands, we're here to meet you where you're at. * Consult with your clinical director and your ...

NCIRE

Staff Research Associate II

San Francisco, CA · On-site +1

Experience with clinical trial management or coordination (e.g., tracking visit windows, managing ... remote PPG from video) is strongly preferred ; enthusiasm for further developing these skills is ...

Lighthouse Autism Center

Clinical Psychologist

$90K - $124K/yr

... a Remote Clinical Psychologist who is passionate about supporting families navigating neurodevelopmental diagnoses. This position offers flexibility to join our team either part-time (minimum 20 ...

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How much do remote clinical trial part time jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for remote clinical trial part time 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 are the key skills and qualifications needed to thrive as a Remote Clinical Trial Coordinator (Part Time), and why are they important?

To thrive as a Remote Clinical Trial Coordinator (Part Time), you need a background in life sciences or healthcare, attention to detail, and an understanding of clinical trial protocols, often supported by a relevant degree or certification such as GCP (Good Clinical Practice). Familiarity with electronic data capture (EDC) systems, remote monitoring platforms, and regulatory documentation tools is essential. Excellent organizational skills, self-motivation, and strong communication are crucial for managing study tasks and collaborating with diverse teams remotely. These competencies ensure the accurate, compliant, and efficient execution of clinical trials in a virtual environment.

What is the difference between Remote Clinical Trial Part Time vs Remote Clinical Research Coordinator?

AspectRemote Clinical Trial Part TimeRemote Clinical Research Coordinator
CredentialsTypically requires a background in healthcare, life sciences, or related field; certifications like CRC or CCRP are a plusRequires similar healthcare or life sciences background; often holds certifications like CRC or CCRP
Work EnvironmentPrimarily remote, flexible hours, often project-basedPrimarily remote, involves coordinating study activities, communicating with sites and sponsors
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, CROs, pharmaceutical companies

Remote Clinical Trial Part Time and Remote Clinical Research Coordinator roles share similar credentials and work environments, often involving remote work in the clinical research industry. The main difference lies in the scope: part-time roles focus on specific trial tasks, while coordinators manage overall study operations.

What are Remote Clinical Trial Part Time jobs?

Remote Clinical Trial Part Time jobs involve supporting clinical research studies from a location outside of a traditional office or clinic, on a part-time schedule. These roles can include tasks such as data entry, patient recruitment, monitoring study compliance, or coordinating with research teams. Working remotely allows for flexibility, making these positions ideal for those who need to balance other commitments. Typical employers include pharmaceutical companies, contract research organizations (CROs), and academic institutions. Candidates often need backgrounds in healthcare, life sciences, or clinical research.

What are some common challenges faced when working remotely on clinical trials part-time, and how can they be managed?

Working remotely on clinical trials part-time often involves challenges such as coordinating effectively with on-site teams, managing time zones, and ensuring timely communication of study data. To overcome these, it's important to establish clear communication protocols, make use of project management tools, and schedule regular check-ins with team members. Staying organized and proactive about potential bottlenecks can help you deliver results efficiently while maintaining work-life balance.
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What cities are hiring for Remote Clinical Trial Part Time jobs? Cities with the most Remote Clinical Trial Part Time 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 job categories do people searching Remote Clinical Trial Part Time jobs look for? The top searched job categories for Remote Clinical Trial Part Time jobs are:
Remote Clinical Trial Part Time jobs near you
Clinical Research Coordinator - Philadelphia, PA

Clinical Research Coordinator - Philadelphia, PA

IQVIA

Philadelphia, PA • Remote

$35 - $42/hr

Part-time

Medical, Life

Posted 28 days ago

IQVIA rating

8.2

Company rating: 8.2 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

46th of 204 rated it services

Job description

Clinical Research Coordinator - Philadelphia, PA

Work Setup: On-site
Employment Type: Part-time - 24 Hours per Week

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with leading pharmaceutical, biotechnology, and medical device organizations to improve patient outcomes and accelerate innovation. By combining deep scientific expertise with cutting-edge technology, we deliver high-quality data and insights that shape the future of clinical trials.

Position Overview

We are seeking a Clinical Research Coordinator (CRC) to support the successful execution of clinical research studies under the direction of a Principal Investigator. This is a hands-on role requiring clinical, operational, and patient-facing expertise to ensure studies are conducted safely, efficiently, and in compliance with regulatory standards.

Key Responsibilities

  • Perform clinical procedures such as ECGs, vital signs, and biological sample collection in accordance with study protocols

  • Coordinate day-to-day clinical trial activities while ensuring compliance with GCP, protocol, and regulatory requirements

  • Prepare study materials, organize equipment, and support overall site readiness

  • Conduct patient recruitment activities, including chart review, phone screening, and scheduling study visits

  • Perform and manage patient study visits in accordance with protocol requirements

  • Educate and orient participants, ensuring a high standard of patient care and safety

  • Accurately collect, document, and enter data into EDC systems and case report forms (CRFs)

  • Resolve data queries in a timely manner and maintain high data quality standards

  • Collaborate with investigators, sponsors, and monitors during site visits and audits

  • Serve as a patient advocate and maintain a safe, compliant clinical environment

Qualifications

  • Bachelor's degree preferred, or an equivalent combination of education and relevant experience

  • Minimum of 1+ years of clinical research experience in a coordinator or similar role

  • Working knowledge of clinical trial processes, GCP guidelines, and medical terminology

  • Proven ability to conduct patient study visits in accordance with protocol requirements

  • Experience in patient recruitment, including chart review and phone screenings

  • Proficiency with EDC systems, including accurate data entry and query resolution

  • Strong attention to detail, organizational skills, and ability to manage multiple priorities

  • Effective communication skills and ability to build collaborative working relationships

  • Cardiovascular research experience preferred

Why Join IQVIA?

  • Be part of a global organization at the forefront of clinical innovation

  • Collaborate with industry-leading experts and researchers

  • Contribute to advancing treatments that improve patient lives

Note: This position is not eligible for visa sponsorship

#LI-CES and #LI-DNP #LI-HCP #remote

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

Pay

Benefits

Hours and flexibility

Workplace

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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