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Clinical Research Data Assistant Jobs in Spring, TX

Forefront Dermatology

Clinical Research Coordinator

Houston, TX · On-site

$23.25 - $30.75/hr

Overview The Clinical Research Coordinator drives clinical research strategy and execution across ... Manage Regulatory Compliance and Data Integrity. Direct preparation and submission of regulatory ...

Care Access

Clinical Research Coordinator II

Houston, TX · On-site

$23.25 - $30.75/hr

Resolve data management queries and correct source data within sponsor provided timelines * Assist ... Minimum Experience: * 3 years prior Clinical Research Coordinator experience required * Prefer 1 ...

Clinical Research Solution LLC

Be Seen First

Clinical Study Coordinator

Houston, TX · On-site

$49K - $59K/yr

Position Summary The Clinical Research Coordinator will support daily clinical trial operations ... Maintain accurate source documentation and eCRF data entry * Manage investigational product ...

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

As of Sep 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 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 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 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 Assistant

Retina Consultants of Texas

Bellaire, TX • On-site

$19/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 14 days ago

Retina Consultants Of Texas rating

7.2

Company rating: 7.2 out of 10

Based on 20 frontline employees who took The Breakroom Quiz

Job description

Overview
Retina Consultants of Texas (RCTX) is seeking a Research Assistant to join our innovative team with the mission of Fighting Blindness For The World To See. This position will be responsible for assisting in research patient visits according to ICH-GCP guidelines and according to the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time. This position will be based at our Bellaire Clinic.
Candidates must be able to meet the needs of the patients and providers, and support the Research Department hours of 6:30am-5pm Monday through Friday. Schedules are provided weekly and are based on the provider's clinic, patient and surgery schedules.
Retina Consultants of Texas is the largest and most respected retina-only ophthalmology practice in the United States. Our group consists of 26 world renowned physicians leading the world in retinal care. While serving two major metropolitan markets (and their extensions) our combined culture allows us to best serve our patients, referral sources and our own team of physicians. RCTX also invests heavily in diagnostic equipment, providing state-of-the-art retina imaging, laser and diagnostic capabilities to each patient. This, combined with the clinical expertise of our physicians, an outstanding and devoted staff, and 25 convenient locations to serve our patients.
We worked hard to create our culture as Retina Warriors. We strongly emphasize our core values of Hard Work, Authentic Care and Innovation in everything we do. It is our belief that by investing in our people, our people will be empowered of their own accord to provide the highest quality patient experience.
In addition to being highly challenged professionally, in joining our practice, the following competitive benefits for full-time eligible employees after a 60-day introductory period:
  • Employee Paid Benefits such as Medical, Dental, and Vision, short-term disability, voluntary life insurance, accident, critical illness, hospital indemnity, pet insurance, HSA pre-taxed contributions, 401 (k) retirement savings contributions both Roth and Traditional options starting date of hire.
  • Employer Paid Benefits such as long-term disability, $25,000 basic life insurance policy, 3% 401(k) safe harbor contribution, HSA employer contributions, annual performance merit increases, certification opportunities, rewards & recognition platform, WellHub Starter Plan Gym Membership, paid time off and (8) paid holidays + (1) floating holiday annually.

Starting Pay Rate is $19.00 per hour and eligible for overtime.
RCTX is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, age, national origin, disability, military service, veteran status, genetic information, or any other protected class under applicable law.
Responsibilities
  • Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines.
  • Prepare visit-specific documentation and charts for Clinical Research Coordinator
  • Inform subjects and obtain written consent in regard to ICF's
  • Assist Coordinator in patient care and management
  • Assist Coordinator in monitoring subject flow and assist in subject care and management
  • Accurately collect and record all necessary data (e.g. demographics, medical history, adverse events, concomitant medications, etc.) during study visit
  • Transcribe subject study information from source documents to the Electronic Case Report Forms
  • Administer all mandatory questionnaires to study subjects
  • Set up, prepare subject, and conduct electrocardiograms on subject who require ECG per study protocol
  • Scribe ocular exams for doctors and confirm appropriate treatment per protocol
  • Promptly request all necessary medical records for Serious Adverse Event Reporting
  • Collection, processing, and shipment of laboratory biological samples for analysis
  • Perform intraocular pressure checks post-injections
  • Review and resolve data management queries as needed
  • Trial frame refraction and ETDRS visual acuity testing
  • Other duties as assigned

Qualifications
Skills/Competencies:
  • Biliginual preferred
  • Ability to multitask
  • Computer efficient
  • Commnucates well both verbally and electronically; email, MS Teams, etc.
  • Detail oriented

Education Requirements
  • Bachelors degree or 4 years of ophthalmic experience in lieu of degree

Experience Requirements:
  • No experience required with a Bachelors degree otherwise at least 4 years of ophthalmic experience

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