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

Associate Director, Team Lead Site Operations Location :FullyRemote Salary Range: $130,000 - $150 ... Proficiencywith clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office ...

Clinical Trial Manager

Houston, TX · On-site

$130K - $150K/yr

Role Overview: We are seeking a Clinical Trial Manager (CTM) to support our U.S. Clinical ... Associate Director, Team Lead Site Operations Location : Fully Remote Salary Range: $130,000 - $150 ...

Study Manager I (3767)

Houston, TX · On-site

$80K - $96K/yr

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 ...

Sub Investigator

Bellaire, TX · On-site

$41K - $42K/yr

Summary: The Clinical Research Nurse Practitioner/Physician Associate will be listed as a sub ... and clinical trial patients. * Coordinates multiple projects with competing priorities and ...

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Clinical Trial Associate information

See Spring, TX salary details

$15

$35

$62

How much do clinical trial associate jobs pay per hour?

As of Jul 17, 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.

How much does a clinical research associate get paid?

A clinical research associate (CRA) typically earns between $60,000 and $110,000 annually, depending on experience, location, and the complexity of trials. Entry-level CRAs may start around $50,000, while experienced professionals with specialized skills can earn over $120,000. Certifications and familiarity with clinical trial management systems can also influence salary levels.

How much do clinical trial associates make in the US?

Clinical Trial Associates in the US typically earn a median annual salary of around $60,000 to $70,000, with entry-level positions starting lower and experienced professionals earning higher wages. Salaries can vary based on location, experience, certifications, and the size of the organization, with some earning over $80,000 annually. The role often requires knowledge of Good Clinical Practice (GCP) guidelines and familiarity with clinical trial management systems.

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.

What does a clinical trials associate do?

A clinical trials associate supports the planning, coordination, and management of clinical studies to ensure they follow regulatory guidelines and protocols. They handle tasks such as data collection, document preparation, and communication with study sites, often using specialized software. Strong organizational skills and knowledge of Good Clinical Practice (GCP) are essential for this role.

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 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 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.

Is CRA an entry level job?

A Clinical Trial Associate (CTA) is typically an entry-level position in clinical research, often suitable for candidates with a bachelor's degree in life sciences or related fields. While some organizations may require prior experience or certifications like GCP training, many CTAs start with on-the-job training and develop skills in trial coordination, documentation, and regulatory compliance.

What are the key skills and qualifications needed to thrive as a Clinical Trial Associate, and why are they important?

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 the most commonly searched types of Clinical Trial jobs in Spring, TX? The most popular types of Clinical Trial jobs in Spring, TX are:
What are popular job titles related to Clinical Trial Associate jobs in Spring, TX? For Clinical Trial Associate jobs in Spring, TX, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Associate jobs in Spring, TX look for? The top searched job categories for Clinical Trial Associate jobs in Spring, TX are:
What cities near Spring, TX are hiring for Clinical Trial Associate jobs? Cities near Spring, TX with the most Clinical Trial Associate job openings:
Infographic showing various Clinical Trial Associate job openings in Spring, TX as of July 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $74,012 per year, or $35.6 per hour.

$130K - $150K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 22 days ago


Job description

JoinImmaticsandshape thefuture ofcancerimmunotherapy; one patient at atime!

Immaticsis committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting ofPRAME, a target expressed in more than 50 cancers. Ourcutting-edgescience and robust clinical pipeline form the broadestPRAMEfranchise with the mostPRAMEindications and modalities, spanning TCR T-cell therapies and TCRbispecifics.

Why Join Us?

  • Innovative Environment:Helptopioneeradvancementsin cancer immunotherapy.

  • Collaborative Culture:Be part ofa diverse team dedicated to your professionalgrowth.

  • Global Impact:Contributeto therapies thatmakealasting impactonpatientsglobally.

Role Overview:

We are seeking a Clinical Trial Manager (CTM) to support our U.S. Clinical Operations team. The CTM will oversee site management, monitoring oversight, and clinical trial operations activities to ensure compliance with GCP, regulatory requirements, and company SOPs. In this role, you will work closely with cross-functional teams and clinical sites to drive study execution, site engagement, and operational excellence across clinical trials.


Reports to:Associate Director, Team Lead Site Operations
Location:FullyRemote

Salary Range:$130,000 - $150,000

Basic Qualifications:

  • Bachelor's degree in life sciences, nursing, or a related field

  • 2+ years of experience in on-site clinical monitoring and 2+ years of Clinical Trial Manager experience within the pharmaceutical or biotechnology industry

  • Strong knowledge of ICH-GCP, FDA, EMA, and applicable clinical trial regulations

  • Demonstrated experience managing clinical trial sites, monitoring activities, and regulatory documentation

  • Proficiencywith clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office)

PreferredQualifications:

  • Experience in oncology clinical trials or related therapeutic areas

  • Advanced ability to manage complex clinical operations processes and drive operational improvements

  • Experience leading training initiatives for CRAs and clinical trial sites

  • Demonstrated ability to drive quality, efficiency, and milestone achievement in fast-paced clinical environments

  • Experience contributing to process harmonization, innovation, and continuous improvement initiatives

  • Strong presentation, organizational, and cross-functional stakeholder management skills

In thisrole youwill:

  • Partner with Clinical Operations leadership to support clinical trial execution and monitoring activities in alignment with project goals

  • Lead site feasibility,selection, initiation, and greenlight activities for clinical trial sites

  • Develop andmaintainstudy-specific operational plans, training materials, and monitoring documentation

  • Oversee site management activities, including site engagement, regulatory submissions, and monitoring oversight

  • Review trial progress, patient recruitment, and data quality metrics, and implement actions to support study objectives

  • Provide guidance and oversight to CRAs, including trip report review and training support

  • Manage protocol and GCP deviations and contribute to continuous improvement of clinical operations processes and procedures

Travel required:up to50% travelrequired, domestically and internationally.

Qualified candidates willparticipatein a structured interview process, which includes:

  • An initialrecruiter phone screen (conducted via video)

  • A recruiter-facilitated introduction and interview with the hiring leader and key stakeholders (via video)

  • A final-stage interview, which may include an in-person meeting at our U.S. Headquarters in Houston, TX

What do we offer?

AtImmatics, we believe in investing in our team's health,safetyand well-being.Here'swhat you can expectif youjoinImmatics

Comprehensive Benefits:

  • Competitive rates forHealth, Dental, and Vision Insurance

  • 4 weeks ofvacation,granted up front each year and prorated for firstand lastyear ofemployment.

  • 12 company paid holidays

  • 7daysof sick time

  • 100%employer-paidlifeinsuranceup toat 1x annual salary, up to one hundred thousand dollars

  • 100%employer-paidshort- andlong-Termdisabilitycoverage

  • 401(k) withimmediateeligibilityandcompany match...

  • The company will match100% of your contributions upto3% of yourbase salaryfor the first two yearsof employment, 4% foryears 2-3 of employment, and up to5%of your salaryfrom the fourth year onward of continued employment.

  • Partiallypaidparentalleavefor eligible employees.

  • Additionalvoluntary employee-paidbenefits and services,includingaccident,hospitalindemnity, andcriticalillnessinsurance, as well as identitytheftprotection andpetinsurance.

Equal Employment Opportunity

We are an equal opportunity employer and are committed to building a diverse and inclusive workplace.We consider all qualified applicants for employment without regard torace, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexualorientation, gender identity or expression, national origin, ancestry, age, marital status, disability, geneticinformation, veteran status, or any other status protected by applicable law.

ReasonableAccommodations

We are committed to providing reasonableaccommodationsto individuals with disabilities and to applicants withsincerely heldreligious beliefs, practices, or observances.If yourequireassistanceoraccommodationduring theapplicationor interview process, please contact us at RecruitingUS@immatics.com.

Equal Employment Opportunity

We are an equal opportunity employer and are committed to building a diverse and inclusive workplace. We consider all qualified applicants for employment without regard torace, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexualorientation, gender identity or expression, national origin, ancestry, age, marital status, disability, geneticinformation, veteran status, or any other status protected by applicable law.

Reasonable Accommodations

We are committed to providing reasonable accommodations to individuals with disabilities and to applicants withsincerely heldreligious beliefs, practices, or observances. If you require assistance or accommodation during the application or interview process, please contact us atRecruitingUS@immatics.com.

Work Authorization

Applicants mustbe authorized towork in the United States without the need for current or future sponsorship. Visa sponsorships may beavailablefor certain roles.

Pre-Employment Requirements

Employment is contingent upon successful completion of a background check, referencechecksand pre-employment drug screening, wherepermittedby applicable law. For certain roles,additionalscreenings such as a credit check or motor vehicle record review may berequired, where job-related and consistent with business necessity.