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Home Based Clinical Research Associate Jobs (NOW HIRING)

Tigermed America

Clinical Research Associate

Denver, CO · On-site

This position is permanent, home-based, must be located in Washington/Oregon/ Colorado/Wyoming/Montana/Utah/Arizona/Idaho/Nevada/New Mexico . Senior Clinical Research Associate As Clinical Research ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

As a Clinical Research Associate at ICON , you will play a pivotal role in designing and analyzing ... based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package ...

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Home Based Clinical Research Associate information

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How much do home based clinical research associate jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for home based clinical research associate in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What are some common challenges faced by Home Based Clinical Research Associates and how can they be managed?

Home Based Clinical Research Associates (CRAs) often face challenges such as maintaining effective communication with site staff and sponsors, managing time efficiently, and staying organized while working remotely. To manage these, CRAs typically rely on regular virtual meetings, robust project management tools, and clear documentation practices. Building strong relationships with site teams and proactively addressing issues also helps ensure smooth study progress and data integrity. Adapting to evolving technologies and maintaining self-discipline are key for success in this remote role.

What are the key skills and qualifications needed to thrive as a Home Based Clinical Research Associate, and why are they important?

To thrive as a Home Based Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory requirements (like GCP), and a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, remote monitoring tools, and relevant certifications such as ACRP or SOCRA are typically required. Excellent organizational skills, attention to detail, and strong verbal and written communication are vital for effective remote collaboration and documentation. These skills ensure clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards, even when working remotely.

What is a Home Based Clinical Research Associate?

A Home Based Clinical Research Associate (CRA) is a professional responsible for monitoring clinical trials and ensuring they comply with regulatory requirements, scientific protocols, and Good Clinical Practice guidelines, all while working remotely from home. They communicate with medical sites, review study documentation, and help maintain data integrity and patient safety. This role requires strong organizational and communication skills, as well as the ability to manage multiple tasks independently from a remote setting.

What is the difference between Home Based Clinical Research Associate vs On-Site Clinical Research Associate?

AspectHome Based Clinical Research AssociateOn-Site Clinical Research Associate
Work EnvironmentPrimarily remote, working from home and visiting sites as neededOn-site at clinical trial locations or sites
Required CredentialsTypically requires a clinical research certification, degree in health sciences, and relevant experienceSimilar credentials, often requiring clinical research certification and healthcare background
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and biotech firms for remote monitoring rolesCommon in hospitals, research centers, and on-site clinical trial sites

The main difference between a Home Based Clinical Research Associate and an On-Site Clinical Research Associate lies in their work environment. The home-based role allows remote monitoring and site visits, offering flexibility, while the on-site role involves working directly at clinical trial locations. Both roles require similar credentials and are integral to clinical research, but their daily operations and work settings differ significantly.

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What cities are hiring for Home Based Clinical Research Associate jobs? Cities with the most Home Based Clinical Research Associate job openings:
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What job categories do people searching Home Based Clinical Research Associate jobs look for? The top searched job categories for Home Based Clinical Research Associate jobs are:
Home Based Clinical Research Associate jobs near you
Infographic showing various Home Based Clinical Research Associate job openings in the United States as of June 2026, with employment types broken down into 2% As Needed, 64% Full Time, 28% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Research Associate/Monitor

Futran Tech Solutions Pvt. Ltd.

Remote

Contractor

Posted yesterday

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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