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Cra Monitor Jobs (NOW HIRING)

Upstart

Data Analyst, Home Lending HMDA

OR · On-site +1

Manage HMDA and CRA data integrity reviews, including routine monitoring, exception tracking, and remediation. * Coordinate the annual HMDA Loan/Application Register (LAR) and CRA data submission ...

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CRA II and Senior CRA

Lawrence, KS · Remote

$91K - $114K/yr

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

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CRA II and Senior CRA

Downers Grove, IL · Remote

$91K - $114K/yr

CRA II or Senior CRA (Home-based in U.S.) ICON is a global healthcare intelligence and clinical ... 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

$91K - $114K/yr

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

Solomon Page

Contract CRA

Covington, KY · On-site

$90 - $100/hr

The ideal candidate will have a strong background in site monitoring and clinical trial management ... This is a home-based position for a CRA located in the Midwest/Central U.S. region, with regular ...

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CRA II and Senior CRA

Houston, TX · Remote

$91K - $114K/yr

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

ICON

CRA II and Senior CRA

Downers Grove, IL · On-site

$91K - $114K/yr

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

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CRA II and Senior CRA

Portland, OR · Remote

$91K - $114K/yr

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

IQVIA

CRA 2/Senior CRA

Sacramento, CA

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in ...

IQVIA

CRA 2/Senior CRA

Dallas, TX

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in ...

IQVIA

CRA 2/Senior CRA

New York, NY · On-site

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in ...

IQVIA

CRA 2/Senior CRA

Sacramento, CA

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in ...

IQVIA

CRA 2/Senior CRA

Gilbert, AZ

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in ...

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Showing results 1-20

All JobsCra Monitor Jobs

Cra Monitor information

See salary details

$11K

$79.4K

$137.5K

How much do cra monitor jobs pay per year?

As of Jul 21, 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 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.

Is it hard to get a CRA job?

Securing a CRA (Clinical Research Associate) position can be competitive, often requiring relevant education such as a degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certifications like ACRP or SOCRA can improve job prospects, but entry may be challenging for those without related experience or credentials.

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 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 salary for CRA?

The salary for a CRA (Clinical Research Associate) typically ranges from $55,000 to $95,000 annually, depending on experience, location, and the employer. Entry-level CRAs may start around $50,000, while experienced professionals with specialized skills can earn over $100,000. Certifications like CCRP can also influence salary levels.

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.

How to become a clinical trial monitor?

To become a clinical trial monitor, typically one needs a bachelor's degree in health sciences, nursing, or a related field, along with experience in clinical research. Certification such as the Certified Clinical Research Professional (CCRP) can enhance job prospects, and familiarity with Good Clinical Practice (GCP) guidelines and clinical trial management systems is often required.

What is a CRA monitor?

A CRA monitor is a professional responsible for overseeing clinical trial sites to ensure compliance with regulatory requirements and study protocols. They typically conduct site visits, review documentation, and verify data accuracy, often requiring knowledge of Good Clinical Practice (GCP) and relevant regulations. The role involves travel and collaboration with research teams to ensure trial integrity.
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 July 2026, with employment types broken down into 3% Locum Tenens, 87% Full Time, 3% Part Time, 1% Contract, and 6% Summer. Highlights an 83% Physical, 4% Hybrid, and 13% 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

This job post has expired today. Applications are no longer accepted.

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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