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Work From Home Clinical Research Associate Jobs (NOW HIRING)

Our work helps bridge critical gaps in care, ensuring safe, ethical, and efficient access to ... If you receive a link from Upwage, it is a legitimate part of our application process and helps ...

From clinical trials to regulatory, consulting, and market access, every clinical development ... We take our work personally, we do it with empathy and we're committed to making a difference. Name ...

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Clinical Research Associate - Multi TA/Oncology - US ICON is a global healthcare intelligence and ... Ability to work independently and collaboratively in a fast-paced environment. * Ability to travel ...

Clinical Research Associate - Multi TA/Oncology - US ICON is a global healthcare intelligence and ... Ability to work independently and collaboratively in a fast-paced environment. * Ability to travel ...

Overview Senior Clinical Research Associate US remotely and on-site (80% travel) Emmes Group ... Work From Home Anywhere in the US * Maternal/Paternal Leave * Casual Dress Code & Work Environment ...

Sr. Clinical Research Associate ICON is a global healthcare intelligence and clinical research ... You will have a strong foundation in clinical trial monitoring, with the experience to work ...

Senior Clinical Research Associate - Oncology ICON is a global healthcare intelligence and clinical ... how we work and interact with each other, customers, patients and suppliers. We are currently ...

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Work From Home Clinical Research Associate information

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$36K

$94.3K

$143.5K

How much do work from home clinical research associate jobs pay per year?

As of Aug 13, 2026, the average yearly pay for work from home clinical research associate in the United States is $94,314.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $128,000.00 per year, depending on experience, location, and employer.

What does a work from home clinical research associate do?

A Work From Home Clinical Research Associate (CRA) is responsible for overseeing clinical trials and studies to ensure they are conducted according to protocols, regulatory requirements, and good clinical practice guidelines. Working remotely, CRAs monitor data collection, verify patient records, ensure compliance, and communicate with trial sites primarily through digital tools. They play a vital role in maintaining the integrity of research while providing flexibility to work from home.

What is the difference between Work From Home Clinical Research Associate vs Clinical Trial Coordinator?

AspectWork From Home Clinical Research AssociateClinical Trial Coordinator
CertificationsTypically requires CRA certification or equivalentOften requires certification or relevant experience
Work EnvironmentPrimarily remote, overseeing multiple sites remotelyUsually on-site or hybrid, managing trial logistics
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research centers, clinical sites

Work From Home Clinical Research Associates focus on monitoring clinical trials remotely, ensuring compliance and data integrity, often working for CROs or pharma companies. Clinical Trial Coordinators handle the day-to-day operations at trial sites, coordinating activities and participant management. Both roles require knowledge of clinical protocols but differ mainly in work setting and responsibilities.

How does remote work impact the collaboration and communication of a work from home clinical research associate with site staff and sponsors?

As a Work From Home Clinical Research Associate, effective collaboration and communication with site staff and sponsors are primarily managed through virtual meetings, emails, and specialized clinical trial management software. While remote work offers flexibility, it also requires proactive communication to ensure timely monitoring, issue resolution, and adherence to study timelines. Building strong relationships remotely can be challenging, but leveraging technology, maintaining regular check-ins, and being responsive help foster trust and smooth collaboration. It's important to stay organized and document all interactions thoroughly for regulatory compliance and project continuity.

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

To thrive as a Work From Home Clinical Research Associate, you need a solid background in life sciences, knowledge of clinical trial protocols, and typically a bachelor's degree in a related field. Familiarity with electronic data capture (EDC) systems, regulatory compliance tools, and Good Clinical Practice (GCP) certification are commonly required. Strong organizational skills, self-motivation, and effective remote communication set top performers apart in this role. These skills ensure accurate trial monitoring, regulatory adherence, and seamless collaboration despite the remote work environment.
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Cities with the most Work From Home Clinical Research Associate job openings:

What are the most commonly searched types of Work From Home Clinical Research jobs?

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Infographic showing various Work From Home Clinical Research Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, and 4% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $94,314 per year, or $45.3 per hour.

Senior Clinical Research Associate - Cra

C-Clinical Miami

Miami, FL โ€ข On-site, Remote

Full-time

Re-posted 9 hours ago


Job description

Description
C-Clinical is seeking a Senior Clinical Research Associate to support clinical trials throughout the Miami region. This opportunity is ideal for an experienced clinical research professional who enjoys site interaction, study oversight, and helping ensure clinical trials operate efficiently from startup through closeout. The position combines remote responsibilities with routine on-site monitoring visits, allowing for both flexibility and direct engagement with investigative teams.
The ideal candidate has a strong background in clinical monitoring along with hands-on experience supporting central nervous system studies, including neurology and psychiatry indications. We are looking for someone who can confidently manage site relationships, review study activity with accuracy, and maintain a high standard of regulatory and protocol compliance throughout the trial process.
This position involves ongoing communication with investigators, coordinators, and sponsors while supporting data quality, patient safety, and study timelines across multiple research sites. Strong organizational skills, professionalism, and the ability to manage competing priorities are important within this environment.
C-Clinical values scientific excellence, collaboration, and operational consistency across every study we support. Our team is passionate about contributing to research that can positively impact patient care while creating an environment where experienced clinical professionals can continue to grow and contribute at a high level.
If you are a Senior CRA located in the greater Miami area with strong CNS clinical trial experience and a passion for quality clinical research, we encourage you to apply.
Interested? Apply now.
Responsibilities
$49
Qualifications
$4a