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Clinical Research Data Assistant Jobs in Spring, TX

Green Life Science

Clinical Research Coordinator

Houston, TX · On-site

$23.25 - $30.75/hr

Clinical Research Coordinator | Houston, TX Headcount: 2 Openings We are partnered with a leading ... paper or electronic data capture systems • Track and report adverse events per protocol ...

MD Anderson Cancer Center

Senior Research Nurse

Houston, TX · On-site

$111K - $133K/yr

... data collection and analysis Create user-generated reports and assist with statistical analysis Develop and maintain research databases while meeting project deadlines Patient Care & Clinical Trial ...

MD Anderson

Senior Research Data Coordinator

Houston, TX · Hybrid

$50K/mo

... Assist with developing and utilizing recruitment materials for educational program participants • Collaborate with Information Technology staff to develop and maintain institutional websites • ...

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All JobsClinical Research Data JobsClinical Research Data Assistant JobsClinical Research Data Assistant Jobs in Spring, TX

Clinical Research Data Assistant information

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How much do clinical research data assistant jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for clinical research data assistant in Spring, TX is $20.21, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $23.12 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Research Data Assistant, you need strong attention to detail, data entry accuracy, familiarity with clinical research protocols, and typically an associate’s or bachelor’s degree in a health-related or scientific field. Proficiency in data management systems such as REDCap, EDC platforms, and Microsoft Excel, as well as knowledge of Good Clinical Practice (GCP) guidelines, is often required. Strong organizational skills, clear communication, and the ability to collaborate with research teams make candidates stand out. These skills ensure careful handling of sensitive data, regulatory compliance, and efficient support for clinical research studies.

What does a clinical research data assistant do?

A Clinical Research Data Assistant is responsible for managing and organizing data collected during clinical trials and research studies. They ensure the accuracy, integrity, and confidentiality of data by entering, verifying, and maintaining research records. These professionals also assist with data cleaning, preparing reports, and supporting regulatory compliance. Their work is essential for the successful analysis and reporting of clinical research findings.

What are some typical challenges faced by clinical research data assistants in maintaining data accuracy?

Clinical Research Data Assistants often encounter challenges such as managing large volumes of complex data, ensuring accurate data entry from multiple sources, and adhering to strict regulatory standards. Mistakes can occur if data is not consistently verified or if communication between research teams is lacking, so attention to detail and strong organizational skills are essential. Regular audits, clear documentation procedures, and collaboration with clinical coordinators help address these challenges and maintain data integrity throughout the research process.

What is the difference between Clinical Research Data Assistant vs Clinical Research Coordinator?

AspectClinical Research Data AssistantClinical Research Coordinator
CredentialsTypically requires a high school diploma or associate degree; some roles prefer certification in clinical researchRequires a bachelor's degree, often in health sciences or related field; certification like CCRP is common
Work EnvironmentSupports data entry, management, and documentation in clinical trial settingsManages entire study processes, including patient recruitment, compliance, and coordination
Employer & IndustryHospitals, research institutions, pharmaceutical companiesResearch sites, hospitals, academic institutions

The Clinical Research Data Assistant primarily handles data-related tasks within clinical trials, while the Clinical Research Coordinator oversees the entire study process. Both roles are essential in clinical research but differ in responsibilities and required qualifications.

What are the most commonly searched types of Clinical Research Data jobs in Spring, TX? The most popular types of Clinical Research Data jobs in Spring, TX are:
What are popular job titles related to Clinical Research Data Assistant jobs in Spring, TX? For Clinical Research Data Assistant jobs in Spring, TX, the most frequently searched job titles are:
What job categories do people searching Clinical Research Data Assistant jobs in Spring, TX look for? The top searched job categories for Clinical Research Data Assistant jobs in Spring, TX are:
What cities near Spring, TX are hiring for Clinical Research Data Assistant jobs? Cities near Spring, TX with the most Clinical Research Data Assistant job openings:
Clinical Research Data Assistant jobs near you
Infographic showing various Clinical Research Data Assistant job openings in Spring, TX as of June 2026, with employment types broken down into 1% As Needed, 77% Full Time, 19% Part Time, and 3% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $42,039 per year, or $20.2 per hour.

Clinical Research Coordinator

Green Life Science

Houston, TX • On-site

$23.25 - $30.75/hr

Other

Medical, Dental, Retirement, PTO

Posted 6 days ago

Job description

Clinical Research Coordinator | Houston, TX

Headcount: 2 Openings


We are partnered with a leading clinical research organisation dedicated to delivering high-quality Phase I–IV clinical trial execution. Our client has completed over 5,000 trials with deep expertise in neuroscience, clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders, with affiliate sites across the U.S.


Why join them? Our client offers a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders — plus competitive benefits including medical and dental coverage, a matching 401(k), and paid time off.


About the Role


Our client is seeking 2 Clinical Research Coordinators. The successful candidates will be responsible for the coordination, management, and implementation of clinical trials. Working under the direction of the Principal Investigator and Site Director, you will complete study-related procedures, manage documentation, and ensure compliance with FDA regulations, GCP guidelines, and company SOPs.


Key Responsibilities


• Review and analyse study protocols prior to study start-up

• Manage studies in collaboration with the Principal Investigator, Site Director, and Recruitment Manager

• Screen and enrol subjects; schedule and conduct study visits

• Obtain informed consent from study volunteers

• Maintain accurate, organised, and complete study records

• Enter data via paper or electronic data capture systems

• Track and report adverse events per protocol requirements

• Liaise with sponsors, IRBs, labs, and regulatory organisations

• Support SOP development and study close-out procedures


What We're Looking For


• Former CRC experience required

• High School Diploma required; college degree preferred

• Knowledge of medical terminology and regulatory requirements (GCP/ICH guidelines)

• Strong communication skills — interpersonal, written, and verbal

• Proficiency in Word, Excel, and clinical research applications (e.g. Study Manager)

• Ability to work independently, exercise sound judgement, and adapt in a dynamic environment

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