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Clinical Research Associate Jobs in Channelview, TX

LINQ Research, LLC

Be Seen First

Clinical Research Coordinator (CRC)

Pearland, TX · On-site

$58K - $65K/yr

Clinical Research Coordinator (CRC) LINQ Research, LLC Location: Pearland, TX -0 Onsite Job Type: Full-Time Schedule: Monday-Friday, 8:00 AM-5:00 PM Department: Clinical Research Reports To: Site ...

Texas A&M University

Research Associate

Houston, TX

Job Title Research Associate Agency Texas A&M University Health Science Center Department IBT - CGPM - Ramos Proposed Minimum Salary Commensurate Job Location Houston, Texas Job Type Staff Our ...

Texas A&M University

Research Associate

Houston, TX · On-site

Job Title Research Associate Agency Texas A&M University Health Science Center Department IBT - CGPM - Ramos Proposed Minimum Salary Commensurate Job Location Houston, Texas Job Type Staff Our ...

Tamus

Research Associate

Houston, TX

Job Title Research Associate Agency Texas A&M University Health Science Center Department IBT - CGPM - Ramos Proposed Minimum Salary Commensurate Job Location Houston, Texas Job Type Staff Our ...

FOCUSPOINT

Clinical Research Coordinator

Webster, TX · On-site

Clinical Research Coordinator Location: Multiple Locations - TX, VA, FL Employment Type: Contract - 6 months Pay: Up to $35 per hour About FOCUSPOINT: FOCUSPOINT specializes in connecting top-tier ...

MD Anderson

Clinical Trial Technician

Houston, TX · On-site

$26.44 - $31.73/hr

CCRA - Certified Clinical Research Associate The University of Texas MD Anderson Cancer Center offers excellent benefits, including medical, dental, paid time off, retirement, tuition benefits ...

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All JobsClinical Research Associate JobsClinical Research Associate Jobs in Channelview, TX

Clinical Research Associate information

See Channelview, TX salary details

$10

$35

$60

How much do clinical research associate jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical research associate in Channelview, TX is $35.43, according to ZipRecruiter salary data. Most workers in this role earn between $24.86 and $45.34 per hour, depending on experience, location, and employer.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

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

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
More about Clinical Research Associate jobs

What are the most commonly searched types of Clinical Research jobs in Channelview, TX?

The most popular types of Clinical Research jobs in Channelview, TX are:

What job categories do people searching Clinical Research Associate jobs in Channelview, TX look for?

The top searched job categories for Clinical Research Associate jobs in Channelview, TX are:

What cities near Channelview, TX are hiring for Clinical Research Associate jobs?

Cities near Channelview, TX with the most Clinical Research Associate job openings:

Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Channelview, TX as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $73,703 per year, or $35.4 per hour.

Nurse - Clinical Research Nurse

Tranquil Clinical and Research Consulting Services LLC

Webster, TX • Remote

$60K - $95K/yr

Full-time

PTO

Re-posted 25 days ago

Job description

 

Tranquil Clinical Research cares about the opinion of our employees and we want the world to know what an amazing place Tranquil is to work for. We always do the right thing, our number one job is the rights, safety and well being of our patients, we train hard and we play hard. We know that our employee provides an essential service and therefore we take better care of our employees than any CRO/Phase I unit in the US.

Tranquil Clinical Research offers employees competitive pay for all positions. Each employee receives 16 days of PTO and 6 days of sick/mental health days with all of the major holidays off. 


Job Title: Research Nurse

Department: Clinical Research

Reports to: CNO


Summary

The role of the study Research Nurse is to ensure patient safety and wellbeing.   The Research Nurse will coordinate and perform study visits under the guidance and supervision of the principal investigator.  This is an office-based position.

To be successful in this role, the Research Nurse should be able to perform IV Therapy, phlebotomy, critical patient evaluations, in addition to recognizing logistical problems and initiating appropriate solutions. Ideal candidates will be patient-focused, detail-oriented, have the ability to multitask and be able to collaborate with various role players. The Research Nurse must be able to work independently, be a team player, and proactively problem solve.

Qualifications

  • RN/LVN with related clinical experience
  • Experience working on clinical trials for a minimum of 1 year
  • IV Therapy / Infusion Therapy
  • Accuracy, attention to detail and ability to set priorities and meet deadlines
  • Basic Computer Skills required: Microsoft Office Suite, including Word PowerPoint, Excel
  • Other Skills required:
    1. Excellent bedside manner and patient-centric focus
    2. Excellent time management and social skills
    3. Highly motivated with a phenomenal eye for detail
  • Function as a Research Nurse Study Coordinator