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Clinical Trial Assistant Jobs in Spring, TX (NOW HIRING)

IQVIA

Clinical Trial Rater

Houston, TX · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate Contract based About IQVIA ...

MD Anderson

Clinical Trial Technician

Houston, TX

$26.44 - $31.73/hr

The primary purpose of the Clinical Trial Technician position is to support the execution of ... Laboratory Operations and Collaboration (20%) • Assist with laboratory equipment maintenance ...

New

MD Anderson Center

Clinical Trial Technician

Houston, TX · On-site

$26.44 - $31.73/hr

The primary purpose of the Clinical Trial Technician position is to support the execution of ... Laboratory Operations and Collaboration (20%) • Assist with laboratory equipment maintenance ...

New

MD Anderson

Clinical Trial Technician

Houston, TX

$44K/mo

The primary purpose of the Clinical Trial Technician position is to support the execution of ... Laboratory Operations and Collaboration (20%) • Assist with laboratory equipment maintenance ...

New

Javara

Clinical Trial Navigator II

Conroe, TX

Operate as the lead Clinical Trial Navigator for multiple clinical studies, dependent upon site-specific study needs such as study complexity and enrollment goal volume, by owning the enrollment plan ...

New

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 ... Communicate with sponsors/CROs regarding queries and monitoring visits * Assist with regulatory ...

DM Clinical

Study Manager I (4012)

Houston, TX · On-site

Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator ... * Assist the Associate Site Director/Site Director with staff training and any other relevant ...

MD Anderson

Clinical Trial Technician QAQC

Houston, TX · On-site

$18.25 - $23.50/hr

The Clinical Trial Technician gains hands-on experience in regulated clinical research while ... • Assist with troubleshooting specimen-related issues and protocol deviations Regulatory ...

MD Anderson

Clinical Trial Technician QAQC

Houston, TX · On-site

$18.25 - $23.50/hr

The Clinical Trial Technician gains hands-on experience in regulated clinical research while ... Assist with troubleshooting specimen-related issues and protocol deviations Regulatory Compliance ...

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All JobsClinical Trial JobsClinical Trial Assistant JobsClinical Trial Assistant Jobs in Spring, TX

Clinical Trial Assistant information

See Spring, TX salary details

$10

$33

$61

How much do clinical trial assistant jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for clinical trial assistant in Spring, TX is $33.52, according to ZipRecruiter salary data. Most workers in this role earn between $22.88 and $42.79 per hour, depending on experience, location, and employer.

What is a clinical trial assistant?

Clinical Trial Assistants (CTAs) are professionals who provide administrative support to clinical research teams during the planning, execution, and close-out of clinical trials. They help ensure that studies comply with regulatory standards, maintain accurate documentation, and coordinate communication between different stakeholders. CTAs often manage trial master files, track study progress, and assist with scheduling meetings and site visits. Their work is essential to the smooth operation of clinical studies and the integrity of collected data.

What does a clinical trial assistant do?

A clinical trial assistant is responsible for monitoring the medical and administrative procedures during a clinical trial. In this career, you prepare patients for tests, take blood, perform laboratory work, prep for medical treatments, and collect data for research. You work with project managers and research associates throughout the beginning, implementation, and closeout of the trial. You also handle paperwork, file records, prepare reports, label medication, track progress, and fulfill other duties that arise during medical studies. You may assist with appointment schedules, plan meetings, and communicate with external sources and investigators as well.

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

To thrive as a Clinical Trial Assistant, you need a solid understanding of clinical research processes, attention to detail, and a relevant degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, trial management software, and knowledge of Good Clinical Practice (GCP) guidelines are typically required. Strong organizational skills, effective communication, and the ability to multitask help you excel in supporting clinical trial operations. These skills ensure protocol compliance, data accuracy, and smooth coordination within clinical research teams.

What are some typical challenges a clinical trial assistant may face when supporting multiple trials simultaneously?

Clinical Trial Assistants often support several studies at once, which can make time management and organization challenging. Balancing competing priorities, meeting tight regulatory deadlines, and ensuring accurate documentation are common hurdles. Effective communication with study coordinators, principal investigators, and sponsors is essential to keep all parties informed and processes running smoothly. Proactively using organizational tools and regularly updating tracking systems can help manage this fast-paced environment.

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

AspectClinical Trial AssistantClinical Research Coordinator
ResponsibilitiesSupports trial logistics, manages documentation, assists with regulatory complianceOversees study conduct, recruits participants, manages site operations
CredentialsTypically requires a bachelor's degree in health or life sciencesOften requires a bachelor's or master's degree in health sciences or related fields
Work EnvironmentResearch sites, sponsor offices, clinical trial centersClinical sites, hospitals, research institutions
Industry UsageCommonly employed in pharmaceutical companies, CROs, research institutionsPrimarily in hospitals, clinics, research centers

The Clinical Trial Assistant primarily supports trial logistics and documentation, working closely with the research team. In contrast, the Clinical Research Coordinator manages the overall conduct of the study, including participant recruitment and site management. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

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Clinical Trial Assistant jobs near you
Infographic showing various Clinical Trial Assistant job openings in Spring, TX as of August 2026, with employment types broken down into 2% As Needed, 76% Full Time, 15% Part Time, and 7% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $69,720 per year, or $33.5 per hour.

Clinical Trial Research Assistant

Advanced Rheumatology of Houston

The Woodlands, TX • On-site

$15 - $18/hr

Full-time

Re-posted 27 days ago

Job description

Clinical Trial Research Assistant
The Woodlands, TX | Full-Time | Private Outpatient Medical Clinic/Onsite

Woodlands Private Outpatient Medical Clinic is actively seeking a Clinical Trial Research Assistant to join our dedicated clinical research team. This is an exciting opportunity to be involved in cutting-edge medical research in a supportive and dynamic outpatient setting.

Key Responsibilities:
  • Process and ship biological specimens per study protocol.
  • Maintain lab inventory and order clinical trial supplies.
  • Ensure accurate and complete study documentation in compliance with institutional and federal regulations.
  • Support research coordinators with testing procedures and overall trial conduct.
  • Advertise, screen, recruit, and enroll patients in clinical trials.
  • Obtain informed consent and explain study participation clearly.
  • Schedule appointments, diagnostic tests, and study-related procedures.
  • Assist with data entry into electronic case report forms (eCRFs) and databases.
  • Support the preparation and submission of reports to regulatory bodies (IRB, FDA, DSMB).
  • Maintain knowledge of current study protocols and standard operating procedures.
  • Prepare for monitoring visits, sponsor audits, and regulatory inspections.
  • Help collect and report adverse events.
  • Attend ongoing training and continuing education relevant to research duties.

Preferred Skills:
  • Phlebotomy, ECG/EKG, and vital signs collection preferred (or willingness to be trained).
  • Experience with specimen processing, shipping, and documentation.
  • Bilingual (English/Spanish) is a plus.

Requirements:
  • Bachelor's degree or higher in a science-related field US University (e.g., biology, chemistry, biochemistry).
  • Previous lab experience with biological specimen handling.
  • Proficient in maintaining documentation and adhering to study protocols.
  • MUST live within 30 mins of The Woodlands.
  • THIS POSITION IS ONSITE.
  • Must be Technologically Adept.
  • Strong attention to detail and protocol compliance.
  • Excellent communication and organizational skills.

Why Join Us?
  • Supportive, collaborative team environment.
  • Opportunity to work on innovative, impactful clinical trials.
  • On-the-job training and professional development.
  • Regular weekday schedule with no night or weekend shifts.