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Work From Home Cra Jobs (NOW HIRING)

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Work From Home Cra information

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$11K

$79.4K

$137.5K

How much do work from home cra jobs pay per year?

As of Jul 31, 2026, the average yearly pay for work from home cra in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Work From Home Cra position, and why are they important?

To excel as a Work From Home CRA (Clinical Research Associate), proficiency in clinical research protocols, regulatory compliance, and a bachelor’s degree in life sciences or a related field are essential. Familiarity with electronic data capture (EDC) systems, trial management software, and certifications like GCP (Good Clinical Practice) are typically required. Exceptional organizational skills, attention to detail, and strong written and verbal communication abilities set top performers apart. These skills are critical for ensuring clinical trial quality, maintaining regulatory standards, and effective remote collaboration with sponsors and research sites.

How hard is it to get a CRA job?

Securing a CRA (Clinical Research Associate) position typically requires relevant education, such as a degree in life sciences or healthcare, and experience in clinical trials or related fields. Employers often look for strong organizational skills, knowledge of Good Clinical Practice (GCP), and sometimes certification, making the process competitive but achievable with proper qualifications and experience.

How can I make 2000 a week working from home?

Work From Home CRAs can increase earnings by gaining experience, obtaining relevant certifications, and taking on multiple projects or clients. High-paying opportunities often require strong organizational skills, industry knowledge, and proficiency with remote collaboration tools. Consistent performance and expanding your network can also help reach higher weekly income levels.

What does a typical workday look like for a Work From Home Clinical Research Associate (CRA)?

A typical workday for a Work From Home CRA involves remotely monitoring clinical trial sites, reviewing data for protocol compliance, and preparing visit reports. You’ll communicate frequently with study coordinators, investigators, and your project team through video calls, emails, and trial management platforms. While most tasks can be handled remotely, occasional travel to sites may be required for on-site verification. Balancing independent responsibilities with effective virtual teamwork is key to success in this remote role. The position offers flexibility but requires strong self-motivation and proactive communication.

What jobs pay 4000 a week without a degree?

Work From Home Customer Service Representatives, sales roles, and freelance digital marketers can sometimes earn $4,000 or more weekly, especially with experience, commissions, or high-volume work. These jobs often require strong communication skills, self-motivation, and proficiency with relevant tools or platforms, but typically do not require a formal degree.

Can I work from home as a CRA?

Yes, many Clinical Research Associates (CRAs) can work from home, especially in roles that involve monitoring clinical trials remotely, reviewing data, and communicating with study sites. Remote CRA positions often require strong organizational skills, familiarity with clinical trial management systems, and relevant certifications such as a CCRP or RAC. However, some companies may require occasional site visits or in-person meetings depending on the role and project needs.

What is a Work From Home CRA job?

A Work From Home Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory guidelines and protocols, all while working remotely. They oversee site activities, review trial data, and communicate with investigators and sponsors to ensure the study's integrity. This role typically requires experience in clinical research, knowledge of Good Clinical Practice (GCP), and strong organizational skills. Working remotely, CRAs use technology to conduct virtual site visits and maintain documentation while ensuring adherence to safety and ethical standards.

More about Work From Home Cra jobs
What cities are hiring for Work From Home Cra jobs? Cities with the most Work From Home Cra job openings:
What states have the most Work From Home Cra jobs? States with the most job openings for Work From Home Cra jobs include:
Infographic showing various Work From Home Cra job openings in the United States as of July 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) (LA)

Medpace, Inc.

Los Angeles, CA • Remote

$60K - $140K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 9 days ago


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

14th of 72 rated research


Job description

Job Summary

Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team!

This is an exciting home-based opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully resourced CRA. You will also have the opportunity to earn a generous travel bonus, in addition to a competitive salary.

We Offer the Following: 

  • Competitive travel bonus
  • Equity/Stock option program
  • Training completion and retention bonus
  • Annual merit increases
  • 401K matching
  • Opportunity to work from home
  • Flexible work hours across days within a week
  • Retain airline reward miles and hotel reward points
  • Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere
  • In-house travel agents, reimbursement for airline club membership, and TSA pre-check
  • Opportunity for leadership positions - Lead CRA, CRA Manager, Training and Development Manager, and many more
  • CRA training program - PACE
  • Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
  • In-house administrative support for all levels of CRA
  • Opportunity to work with international team of CRAs
Responsibilities
  • Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol
  • Communication with the medical site staff including coordinators, clinical research physicians, and their site staff
  • Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff
  • Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements
  • On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward
  • Verification the investigator is enrolling only eligible subjects
  • Regulatory document review
  • Medical device and/or investigational product/drug accountability and inventory
  • Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol
  • Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement
  • Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance
Qualifications
  • Minimum of a Bachelor's degree in a health or science related field
  • Experience as a Clinical Research Coordinator (minimum 1 year)
  • Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely
  • A valid driver's license and the ability to drive to monitoring sites
  • Proficient knowledge of Microsoft Office
  • Strong communication and presentation skills
  • Detail-oriented and efficient in time management

Compensation

A target salary range of $60,000 - $140,000 with potential for bonus and equity awards. Your compensation will be based on your skills and experience. Medpace offers the following benefits for full-time positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, pet insurance, and reimbursement for travel expenses (including food and gas allowance, rental cars, and hotel accommodations). For more details, please discuss with your recruiter.

#LI-Remote

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

    • 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, and PTO benefits

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

What Medpace employees say

Pay

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Hours and flexibility

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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