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Clinical Research Monitor Jobs in Spring, TX (NOW HIRING)

Clinical Research Solution LLC

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Clinical Study Coordinator

Houston, TX · On-site

$49K - $59K/yr

Prepare for monitoring visits, audits, and inspections * Required Qualifications * 1+ year of clinical research experience OR strong clinical background Company Description Clinical Research Solution ...

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Clinical Research Coordinator II

Houston, TX · On-site

$23.25 - $30.75/hr

With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring ... Monitors quality metrics; prevents deviations; resolves queries quickly. * Interact in a positive ...

Care Access

Clinical Research Coordinator II

Houston, TX · On-site

$23.25 - $30.75/hr

With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring ... Monitors quality metrics; prevents deviations; resolves queries quickly. * Interact in a positive ...

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Clinical Research Monitor information

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How much do clinical research monitor jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical research monitor in Spring, TX is $34.44, according to ZipRecruiter salary data. Most workers in this role earn between $33.99 and $34.86 per hour, depending on experience, location, and employer.

What is a clinical research monitor?

A clinical research monitor, also called a clinical research associate, oversees the operations of a clinical trial to ensure that it meets all safety and governmental regulations. As a clinical research monitor, your job duties include traveling to testing sites, inspecting the procedures, documenting results from the trial, and verifying that all collected data is accurate and verified. Your primary responsibility is to make sure the testing is conducted safely and within industry and governmental guidelines.

What are the key skills and qualifications needed to thrive as a clinical research monitor?

To thrive as a Clinical Research Monitor, you need a solid understanding of clinical trial protocols, regulatory compliance (such as GCP), and a degree in life sciences or a related field. Familiarity with electronic data capture systems, trial management software, and certifications like ACRP or SOCRA are highly valued. Excellent organizational skills, attention to detail, and effective communication are essential soft skills for managing site relationships and ensuring protocol adherence. These competencies are crucial for safeguarding data integrity, patient safety, and regulatory compliance throughout the clinical trial process.

What are some common challenges clinical research monitors face when overseeing multiple study sites?

Clinical Research Monitors often encounter challenges such as managing varying levels of compliance across different sites, coordinating communication between site staff and sponsors, and ensuring timely data collection and reporting. Travel between sites and adapting to diverse protocols or site-specific processes can also present logistical hurdles. Successful monitors develop strong organizational skills, maintain meticulous documentation, and build collaborative relationships with site teams to navigate these challenges effectively.

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

AspectClinical Research MonitorClinical Research Associate
CertificationsOften required or preferred certifications like CCRP or CCRASimilar certifications such as CCRP or CCRA are common
Work EnvironmentMonitoring visits at sites, reviewing data, ensuring complianceSite visits, data collection, and regulatory documentation
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms

Both roles involve overseeing clinical trial activities, ensuring compliance, and maintaining data integrity. While the titles are often used interchangeably, the term 'Clinical Research Monitor' emphasizes the monitoring aspect, whereas 'Clinical Research Associate' may encompass broader responsibilities in clinical trial management. Both roles require similar certifications and work in comparable environments within the industry.

What does a clinical research monitor do in clinical research?

A clinical research monitor oversees the progress of clinical trials to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. They conduct site visits, review data for accuracy, and verify that trial procedures are followed correctly, often using electronic data capture systems. Monitoring is essential for maintaining data integrity and participant safety throughout the study.
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Clinical Research Monitor jobs near you
Infographic showing various Clinical Research Monitor job openings in Spring, TX as of August 2026, with employment types broken down into 3% As Needed, 73% Full Time, 17% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $71,636 per year, or $34.4 per hour.

Clinical Study Coordinator

Clinical Research Solution LLC

Houston, TX • On-site

$49K - $59K/yr

Full-time

Medical

Posted 24 days ago

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Job description

Position Summary

The Clinical Research Coordinator will support daily clinical trial operations, including patient visits, regulatory compliance, data entry, and sponsor communication. This role requires strong organizational skills, attention to detail, and the ability to work in a fast‐paced research environment.

Key Responsibilities

  • Conduct and document study visits per protocol, GCP, and site SOPs
  • Coordinate patient scheduling, screening, enrollment, and follow‐up
  • Collect, process, and ship biological samples (blood, urine, plasma)
  • Maintain accurate source documentation and eCRF data entry
  • Manage investigational product accountability
  • Communicate with sponsors/CROs regarding queries and monitoring visits
  • Assist with regulatory submissions, logs, and essential documents
  • Ensure protocol adherence and patient safety at all times
  • Support recruitment efforts and pre‐screening activities
  • Prepare for monitoring visits, audits, and inspections
  • Required Qualifications
  • 1+ year of clinical research experience OR strong clinical background

Company Description

Clinical Research Solution LLC conducts clinical trials at the doctor offices