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Work From Home Clinical Research Associate Jobs (NOW HIRING)

Ora

Senior Clinical Research Associate

Our Sr. CRA's will work with the oversight of the Lead CRA and Line Manager. As a Sr. CRA, you will ... Responsibilities may differ from the above based on the specific needs of the business What We Look ...

ICON

Clinical Research Associate

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 ...

ICON

Clinical Research Associate

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 ...

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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 Jun 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 are synonyms for work?

Synonyms for work include terms like employment, job, occupation, position, task, duty, and role. For a Work From Home Clinical Research Associate, these words relate to the professional activities and responsibilities involved in conducting clinical trials and managing study protocols remotely.

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.

What is the meaning of work?

Work, including roles like a Work From Home Clinical Research Associate, refers to the effort or activity performed to achieve a specific goal, often involving tasks, responsibilities, and skills. In a professional context, it typically involves applying knowledge and tools to complete assignments, often within a schedule or set of standards.

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, and why are they important?

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.

What does the slang work mean?

In the context of a Work From Home Clinical Research Associate role, 'work' refers to the tasks and responsibilities involved in managing clinical trials, such as monitoring study sites, ensuring compliance, and collecting data. It typically involves using specialized software, adhering to protocols, and maintaining communication with team members remotely.

What is the 3 3 3 rule at work?

The 3 3 3 rule in a Work From Home Clinical Research Associate role typically refers to a time management guideline, suggesting that tasks or meetings should be limited to three minutes, three hours, or three days to maintain productivity and focus. It helps remote professionals prioritize and avoid burnout by setting clear boundaries for communication and task completion.
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Work From Home Clinical Research Associate jobs near you
Infographic showing various Work From Home Clinical Research Associate job openings in the United States as of June 2026, with employment types broken down into 65% Full Time, and 35% Part Time. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $94,314 per year, or $45.3 per hour.

Clinical Research Associate/Monitor

Futran Tech Solutions Pvt. Ltd.

Remote

Contractor

Posted 19 hours ago

Job description

Job Title: Clinical Research Associate/Monitor
6 months contract to perm
Work location: REMOTE
Required 30%-50% traveling
Candidate home location: required within DC, VA, MD only (a candidate needs to reside in DC, VA, MD)
Multiple Regional CRAs: 5 openings
USC/GC required
Search Term: Regional CRA, Contract CRA, Sr. CRA, Home-based CRA, Regional Clinical Research Associate, Regional CRA III, Sr. Clinical Research Associate, Senior Clinical Research Associate, Monitor, Contract CRA II, CRA III, Regional Monitor, Home-based Regional CRA, CRA, Contract Clinical Research Associate, Regional CRA Consultant, Phase I, Study Monitor, Contract Monitor, CRA, Research Associate
Multiple Studies with Health patients - Previous Phase I experience required
Contract CRAs, regional based with strong monitoring skills, minimum 3-5+ years monitoring experience within the pharmaceutical industry required traveling of minimum of 50% traveling to 1-2 sites within the same state as required. Require 100% commitment and contractors paid hourly. Therapeutic areas can range and candidates will be expected on working on about 6-8 protocols (max at 10 protocols) with different indications. Multiple sites and candidate has to be local to DC, VA, and MD areas.
Minimum 3-5+ years of CRA / Monitoring experience required
Start date is ASAP
TRAVEL INFORMATION FOR CANDIDATES -
The client is working to ensure candidates are as close as possible to their sites. Company is constantly adding new studies to the monitoring project. Monitors may be asked to take on additional sites closer to their home (or maybe a bit further then what they currently have) - they will work to keep travel as regionally located as possible. There are multiple sites in each region (depends on the allocation of the individual CRAs)
In addition they should be very clear about their monitoring experience showing that they are a Regional CRA/monitor currently. (I would say 3 years monitoring experience with Oncology study required) Candidates need to allocate 50% to 100% of their time to this assignment, preferred candidates home is close to the site locations (listed above).The CRA/Study Monitor designated activities include site visits, trial monitoring, tracking, documentation, collection, solicitation and review of (e) CRFs and submit data, preparation of reports, regulatory review and participation in teleconferences. Approximately 50% travel will be required, as the CRA Study Monitor's primary responsibilities will be monitoring of study sites.
Requirements
A strong healthcare background with at least 1-2 years prior monitoring Oncology study experience is required. Phase I research experience as a monitor, auditor, research coordinator, research associate or similar oncology research experience is required. The CRA/Study Monitor must hold a Bachelor's degree from an accredited college or University or be a grad from an accredited school of nursing.
Requirement:
  • 2+ years prior monitoring Oncology study experience is required. preferred. Phase I-IV research experience as a monitor, clinical research associate experience is required.
  • BS/BA in life sciences or health-related discipline, BSN, Bachelor of Science - Nursing, Pharmacy is highly desirable.
  • Minimum 3-5+ years clinical research monitoring experience including years in Phase I studies.
  • Strong working knowledge of GCPs, ICH Guidelines, and FDA Regulations
  • Ability and willingness to travel up to 50 % of the time, including minimum overnight stays travel as necessary
  • Experience with regulatory document review/collection and IRB submissions (including OHRP regulations), a plus
  • Experience with using a Trial Master File, a plus.

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