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

Lumiresearch

PRN - Clinical Trial PharmD

Houston, TX · On-site

$100 - $130/hr

The primary purpose of the Clinical Trial PharmD is to provide oversight for investigational drug services across ongoing and upcoming clinical trials. This role is responsible for ensuring the safe ...

MD Anderson

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 ... Associate's Degree in Public Health, Healthcare Administration, or a related scientific field ...

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 ... Associate's Degree in Public Health, Healthcare Administration, or a related scientific field • ...

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 ... Associate's Degree in Public Health, Healthcare Administration, or a related scientific field • ...

MD Anderson

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 ... Associate's Degree in Public Health, Healthcare Administration, or a related scientific field • ...

MD Anderson

Clinical Trial Technician

Houston, TX · On-site

$44K/mo

The primary purpose of the Clinical Trial Technician position is to support the execution of ... Associate's Degree in Public Health, Healthcare Administration, or a related scientific field • ...

Javara

Clinical Trial Navigator II

Conroe, TX · On-site

Associates or Bachelor's Degree in related field or equivalent industry experience. * 2+ years of experience in clinical research that includes hands-on application of clinical functions such as ...

Immatics NV

Senior Clinical Research Associate

Houston, TX · On-site

$120K - $135K/yr

The Senior CRA will be responsible for overseeing clinical trial site management and monitoring ... Associate Director, Team Lead Site Operations Location : Fully Remote Salary Range: $120,000 to ...

DM Clinical

Study Manager I (4012)

Houston, TX · On-site

Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...

Dm Clinical Research Group

Study Manager I

Houston, TX · On-site

$85 - $120/hr

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 tasks ...

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 ... Associate's Degree Public Health, Healthcare Administration or related scientific field. Preferred:

Icon plc

Clinical Research Associate II

Houston, TX · Remote

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

Icon plc

Senior CRA

Houston, TX · On-site

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects ...

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Clinical Trial Associate information

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$62

How much do clinical trial associate jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical trial associate in Spring, TX is $35.58, according to ZipRecruiter salary data. Most workers in this role earn between $28.65 and $39.13 per hour, depending on experience, location, and employer.

What is a clinical trial associate?

A clinical trial associate helps oversee late-stage drug trials. They design and implement the final clinical study before making reports to the FDA and other regulatory bodies. Their duties cover logistics, including ordering supplies, auditing all reports and documents, and ensuring their timely completion. They are responsible for making sure that the trial follows all ICH and GCP requirements.

What does a clinical trial associate do?

A Clinical Trial Associate (CTA) is responsible for supporting the planning, coordination, and management of clinical trials. They help ensure studies comply with regulatory requirements and assist in maintaining trial documentation, tracking study progress, and communicating with clinical sites. CTAs work closely with clinical research teams, sponsors, and vendors to keep trials running smoothly and efficiently. Their administrative and logistical support is essential for successful clinical research.

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

To thrive as a Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines, and a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, CTMS (Clinical Trial Management Systems), and GCP (Good Clinical Practice) certification are commonly required. Attention to detail, strong organizational skills, and effective communication set top performers apart in this role. These competencies are crucial for ensuring compliance, accurate data management, and smooth coordination of clinical trial activities.

What are some common challenges faced by clinical trial associates when managing study documentation?

Clinical Trial Associates often encounter challenges related to maintaining accurate and up-to-date trial documentation, as protocols and regulatory requirements can change frequently. Ensuring all documents are correctly filed, version-controlled, and accessible for audits requires strong attention to detail and organizational skills. Additionally, coordinating with multiple stakeholders—such as clinical research coordinators, data managers, and regulatory teams—can add complexity to document management. Proactive communication and adopting robust documentation systems can help overcome these challenges.

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

AspectClinical Trial AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRABachelor's degree in health sciences or related field; similar certifications
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospital, academic medical centers, clinical trial sites
ResponsibilitiesAssist in trial setup, data collection, regulatory complianceManage patient recruitment, conduct visits, data entry
Industry UsageCommon in pharmaceutical and biotech industriesCommon in hospitals and academic research settings

Both roles support clinical trials but differ mainly in scope and setting. Clinical Trial Associates typically work in industry settings focusing on trial logistics and compliance, while Clinical Research Coordinators often manage patient interactions and data at clinical sites. Understanding these differences helps in choosing the right career path or job search focus.

More about Clinical Trial Associate jobs

What are the most commonly searched types of Clinical Trial jobs in Spring, TX?

The most popular types of Clinical Trial jobs in Spring, TX are:

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For Clinical Trial Associate jobs in Spring, TX, the most frequently searched job titles are:

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What cities near Spring, TX are hiring for Clinical Trial Associate jobs?

Cities near Spring, TX with the most Clinical Trial Associate job openings:

Clinical Trial Associate jobs near you
Infographic showing various Clinical Trial Associate 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 $74,012 per year, or $35.6 per hour.

PRN - Clinical Trial PharmD

Lumiresearch

Houston, TX • On-site

$100 - $130/hr

Other

Posted 5 days ago

Job description

The primary purpose of the Clinical Trial PharmD is to provide oversight for investigational drug services across ongoing and upcoming clinical trials. This role is responsible for ensuring the safe handling, storage, dispensing, and documentation of investigational products in compliance with study protocols, sponsor requirements, and regulatory standards.

This is a flexible, as-needed position ideal for an experienced pharmacist with a background in clinical research, oncology, or infusion services.
May travel to satellite sites if needed for drug delivery in the Greater Houston area.

Requirements:
  • Proficient in pharmacy practice
  • Able to work independently using past knowledge acquired through experience
  • Think critically and quickly to resolve any logistical problems
  • Able to work in an organized manner and follow up with pending items
  • Able to multitask and use resources efficiently
  • Able to work in a team environment
  • Able to work in a startup capacity that can involve exposure to uncertain situations, context and priority changes
Qualifications:
  • Oversee investigational product (IP) management, including receipt, storage, temperature monitoring, labeling, dispensing, and returns/destruction
  • Ensure compliance with study protocols, good clinical practice (GCP), and applicable regulatory standards
  • Maintain accurate and complete drug accountability logs and documentation
  • Create and maintain pharmacy related SOPs
  • Review and verify study prescriptions and dosing instructions for protocol adherence
  • Collaborate with investigators, clinical research coordinators, sponsors, and CROs to support study execution
  • Create patient-friendly handouts if needed/requested to ensure strict drug compliance
  • Assist with site initiation visits (SIVs), monitoring visits, and audits/inspections.
  • Provide guidance on pharmacy-related protocol requirements and investigational drug handling
  • Support staff training in investigational product procedures and workflows
  • Provides drug information to physicians, nurses, and other health care professionals, as related to clinical investigational trial drug
  • Manage and document temperature excursions and protocol deviations
  • Help ensure ongoing pharmacy readiness for sponsor and regulatory audits
  • Business Development
    • Creates new inventory system to maximize revenue
    • Builds new inventory plan according to pipeline of trials
    • Plans all treatments for every patient on a clinical trial, ensures drug availability
  • Complies with all legal requirements and company policies
  • Performs all other duties assigned

Education: Doctor or Pharmacy Degree
Location: Greater Houston Area
Experience: 8 years total; 5 years of pharmacy technician and 3 years in oncology practice
Base Salary: Based Upon Experience

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