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

As of Jun 9, 2026, the average yearly pay for from home cra monitor 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 some common challenges faced by a Work From Home CRA Monitor and how can they be managed?

As a Work From Home CRA (Clinical Research Associate) Monitor, one of the main challenges is maintaining effective communication with on-site staff and ensuring data integrity remotely. Without being physically present, it can be harder to build rapport and quickly resolve site issues. Utilizing robust virtual meeting tools, scheduling regular check-ins, and ensuring thorough documentation can help overcome these challenges. Adapting to new technologies and being proactive in communication are key to success in this remote role.

What are Work From Home CRA Monitors?

Work From Home CRA (Clinical Research Associate) Monitors are professionals who oversee clinical trials and research studies remotely. They ensure that clinical sites comply with protocols, regulatory requirements, and good clinical practice guidelines. By working from home, CRAs use digital tools to monitor data, communicate with site staff, and manage documentation, reducing the need for frequent on-site visits. This role requires strong organizational, communication, and technical skills to maintain the integrity of clinical research while working remotely.

What are the key skills and qualifications needed to thrive as a Home-based Clinical Research Associate (CRA) Monitor, and why are they important?

To thrive as a Home-based CRA Monitor, you need a solid background in life sciences or a related field, previous clinical research experience, and knowledge of Good Clinical Practice (GCP) guidelines. Familiarity with electronic data capture (EDC) systems, remote monitoring tools, and regulatory documentation is typically required, along with relevant certifications such as ACRP or SOCRA. Strong organizational skills, attention to detail, self-motivation, and effective communication are crucial soft skills for managing remote responsibilities and collaborating with study sites. These skills ensure the quality and compliance of clinical trials while enabling efficient remote oversight and accurate reporting.
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From Home Cra Monitor jobs near you
Infographic showing various From Home Cra Monitor job openings in the United States as of June 2026, with employment types broken down into 99% Full Time, and 1% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

Clinical Research Associate/Monitor

Futran Tech Solutions Pvt. Ltd.

Remote

Contractor

Posted 26 days 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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