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Cra Monitor Jobs (NOW HIRING)

TexasBank

CRA Analyst

Fort Worth, TX · On-site

Monitor and track CRA-qualified activities to ensure accurate documentation and reporting * Assist with CRA exams and audits, including responding to information and documentation request * Conduct ...

Orison Solutions

CRA- Analyst

Minneapolis, MN · On-site

$30 - $32/hr

Evaluate, monitor, and document study results. * Exercise good clinical judgment and demonstrate ... In-house pharma CRA experience (strictly Regional CRA experience will be considered) * Clinical ...

Orison

CRA- Analyst

Minneapolis, MN · On-site

Evaluate, monitor, and document study results. * Exercise good clinical judgment and demonstrate ... In-house pharma CRA experience (strictly Regional CRA experience will be considered) * Clinical ...

Seacoast National Bank

HMDA CRA Analyst II

Tampa, FL · On-site

Oversight and monitoring of CRA service hour volumes and reporting accuracy. * Promoting and coordinating bank-wide volunteer opportunities through events module. * Partnering with internal teams and ...

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CRA II and Senior CRA

Portland, OR · Remote

CRA II/Senior CRA (Home-based anywhere in the U.S.) ICON is a global healthcare intelligence and ... Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

ICON plc

CRA II and Senior CRA

Blue Bell, PA · Remote

CRA II/Senior CRA (Home-based anywhere in the U.S.) ICON is a global healthcare intelligence and ... Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

Seacoast National Bank

HMDA CRA Analyst II

Miami, FL · On-site

Oversight and monitoring of CRA service hour volumes and reporting accuracy. * Promoting and coordinating bank-wide volunteer opportunities through events module. * Partnering with internal teams and ...

Seacoast National Bank

HMDA CRA Analyst II

Naples, FL · On-site

Oversight and monitoring of CRA service hour volumes and reporting accuracy. * Promoting and coordinating bank-wide volunteer opportunities through events module. * Partnering with internal teams and ...

Seacoast National Bank

HMDA CRA Analyst II

Orlando, FL · On-site

Oversight and monitoring of CRA service hour volumes and reporting accuracy. * Promoting and coordinating bank-wide volunteer opportunities through events module. * Partnering with internal teams and ...

Seacoast National Bank

HMDA CRA Analyst II

Stuart, FL · On-site

Oversight and monitoring of CRA service hour volumes and reporting accuracy. * Promoting and coordinating bank-wide volunteer opportunities through events module. * Partnering with internal teams and ...

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CRA II and Senior CRA

Blue Bell, PA · Remote

CRA II/Senior CRA (Home-based anywhere in the U.S.) ICON is a global healthcare intelligence and ... Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

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CRA II and Senior CRA

Salt Lake City, UT · Remote

CRA II/Senior CRA (Home-based anywhere in the U.S.) ICON is a global healthcare intelligence and ... Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

ICON

CRA II and Senior CRA

Blue Bell, PA · On-site

CRA II/Senior CRA (Home-based anywhere in the U.S.) ICON is a global healthcare intelligence and ... Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

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Cra Monitor information

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$11K

$79.4K

$137.5K

How much do cra monitor jobs pay per year?

As of Jun 2, 2026, the average yearly pay for 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 the key skills and qualifications needed to thrive as a CRA (Clinical Research Associate) Monitor, and why are they important?

To thrive as a CRA Monitor, you need a solid understanding of clinical trial protocols, regulatory guidelines (such as GCP), and a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are commonly required. Strong attention to detail, communication, and problem-solving skills help build trust with site staff and ensure trial integrity. These skills ensure accurate data collection, regulatory compliance, and the smooth progress of clinical trials.

What are some common challenges Clinical Research Associate (CRA) Monitors face when working across multiple study sites?

CRA Monitors often juggle several clinical trial sites simultaneously, which can present challenges such as coordinating schedules, ensuring consistent protocol adherence, and managing diverse site staff. They need to be adept at prioritizing tasks, maintaining detailed documentation, and swiftly resolving site-specific issues. Effective communication and strong organizational skills are crucial for building good relationships with site staff and ensuring that trials progress smoothly and compliantly.

What are CRA Monitors?

CRA Monitors, also known as Clinical Research Associates (CRAs), are professionals responsible for overseeing clinical trials to ensure they are conducted in accordance with regulatory requirements, study protocols, and ethical guidelines. They act as the main point of contact between the study sponsor and the research sites, monitoring patient safety, data accuracy, and compliance throughout the trial. Their duties include site visits, reviewing case report forms, and ensuring proper documentation, ultimately ensuring the integrity and quality of clinical research.

What is the difference between Cra Monitor vs Clinical Research Associate?

AspectCra MonitorClinical Research Associate
CertificationsTypically requires GCP training, CRA certification (e.g., SOCRA, ACRP)Same certifications as Cra Monitor, often with additional site management training
Work EnvironmentPrimarily monitors clinical trials remotely or on-site at sitesWorks on-site at clinical trial sites, overseeing patient recruitment and data collection
Employer & Industry UsageUsed by pharmaceutical companies, CROs, biotech firmsCommonly employed by CROs, pharmaceutical companies, and research institutions

The Cra Monitor and Clinical Research Associate roles are closely related, with both requiring similar certifications and working within the clinical trial industry. The main difference lies in their focus: Cra Monitors primarily oversee trial compliance and data integrity, often remotely, while Clinical Research Associates are more involved in site management and patient interactions on-site. Both roles are essential in ensuring the success of clinical studies.

More about Cra Monitor jobs
What are the most commonly searched types of Cra Monitor jobs? The most popular types of Cra Monitor jobs are:
What job categories do people searching Cra Monitor jobs look for? The top searched job categories for Cra Monitor jobs are:
Cra Monitor jobs near you
Infographic showing various Cra Monitor job openings in the United States as of May 2026, with employment types broken down into 7% Full Time, 11% Temporary, and 82% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% 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 19 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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