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Clinical Study Assistant Jobs in Texas (NOW HIRING)

HR Anew

Clinical Research Coordinator

Fort Worth, TX · On-site

$45K - $55K/yr

Perform or assist with specimen collection including blood draws * Process and document samples according to protocol requirements Data and Documentation * Enter clinical study data into Electronic ...

HR Anew

Clinical Research Coordinator

Fort Worth, TX · On-site

$45K - $55K/yr

Perform or assist with specimen collection including blood draws * Process and document samples according to protocol requirements Data and Documentation * Enter clinical study data into Electronic ...

New

Adams Clinical

Clinical Research Assistant

Desoto, TX · On-site

$19.23 - $23.08/hr

The Clinical Research Assistant (RA) provides foundational support in the conduct of clinical ... Support study start-up activities, including supply inventory, document preparation, and site ...

Adams Clinical

Clinical Research Assistant

Desoto, TX · On-site

$19.23 - $23.08/hr

The Clinical Research Assistant (RA) provides foundational support in the conduct of clinical ... Support study start-up activities, including supply inventory, document preparation, and site ...

Adams Clinical

Clinical Research Assistant

Desoto, TX · On-site

$19.23 - $23.08/hr

The Clinical Research Assistant (RA) provides foundational support in the conduct of clinical ... Support study start-up activities, including supply inventory, document preparation, and site ...

SGS

Clinical Research Coordinator II

Richardson, TX · On-site

$22 - $29/hr

Sets up and conducts study in compliance with protocol, SOPs, applicable regulations and GCPs ... Initiate electronic questionnaire creation * Assist in IRB and Regulatory Document submission ...

DiaSorin

Clinical Research Associate

Austin, TX · On-site

Create clinical study document designs and tracking tools. * Investigate queries, monitor ... Contribute to the writing of study protocols and reports. * Assist with site contracts and budge ...

DiaSorin

Clinical Research Associate

Austin, TX · On-site

Create clinical study document designs and tracking tools. * Investigate queries, monitor ... Contribute to the writing of study protocols and reports. * Assist with site contracts and budge ...

Baylor Scott & White Health

Research RN 1

Dallas, TX · On-site

You'll develop skills to effectively use the Study Assistant Clinical Trials Management System, as per departmental requirements. Key Success Factors Clinical & Professional Skills * Active RN ...

Baylor Scott & White Health

Research RN 1

Irving, TX · On-site

You'll develop skills to effectively use the Study Assistant Clinical Trials Management System, as per departmental requirements. Key Success Factors Clinical & Professional Skills * Active RN ...

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All JobsClinical Study JobsClinical Study Assistant JobsClinical Study Assistant Jobs in Texas

Clinical Study Assistant information

See Texas salary details

$10

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How much do clinical study assistant jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical study assistant in Texas is $18.85, according to ZipRecruiter salary data. Most workers in this role earn between $15.43 and $21.73 per hour, depending on experience, location, and employer.

What is a clinical study assistant?

Clinical Study Assistants are professionals who support the conduct of clinical trials by handling administrative tasks, maintaining study documentation, and ensuring regulatory compliance. They work closely with clinical research teams to coordinate schedules, communicate with study sites, and help manage trial materials. Their role is crucial in ensuring that clinical studies run smoothly, efficiently, and according to protocols and regulatory guidelines.

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

To thrive as a Clinical Study Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or related fields, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation processes is typically required. Effective communication, teamwork, and problem-solving skills help you navigate complex study protocols and collaborate with diverse stakeholders. These abilities are crucial for ensuring the accuracy, compliance, and smooth operation of clinical research studies.

What are the main challenges a clinical study assistant might face when supporting clinical trial operations?

A Clinical Study Assistant often encounters challenges such as managing multiple tasks under tight deadlines, ensuring accurate documentation, and coordinating communication between research teams, sponsors, and regulatory bodies. Additionally, adapting to evolving study protocols and maintaining compliance with strict regulatory requirements can be demanding. Strong organizational skills, attention to detail, and proactive communication are essential for navigating these challenges successfully.

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

AspectClinical Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree, often with additional certifications in clinical research
Work EnvironmentSupports clinical trials in hospitals, research centers, or pharmaceutical companiesManages entire clinical studies, coordinating between sites, staff, and sponsors
Employer & IndustryHospitals, research institutions, pharmaceutical companiesAcademic medical centers, hospitals, research organizations
Search & Comparison IntentOften compared for entry-level roles supporting clinical trialsCompared for roles with broader responsibilities in clinical study management

The Clinical Study Assistant primarily supports clinical trial activities by assisting with data collection and documentation, while the Clinical Research Coordinator manages the overall conduct of the study, including patient recruitment and compliance. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

What are the most commonly searched types of Clinical Study jobs in Texas?

The most popular types of Clinical Study jobs in Texas are:

What cities in Texas are hiring for Clinical Study Assistant jobs?

Cities in Texas with the most Clinical Study Assistant job openings:

Clinical Study Assistant jobs near you
Infographic showing various Clinical Study Assistant job openings in Texas as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 15% Part Time, 8% Contract, and 1% Nights. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $39,203 per year, or $18.8 per hour.

Clinical Research Coordinator

HR Anew

Fort Worth, TX • On-site

$45K - $55K/yr

Full-time

Re-posted 28 days ago

Job description

Clinical Research Coordinator

Prime Clinical Research

Location: On-Site
Employment Type: Full-Time
Department: Clinical Operations

Prime Clinical Research is seeking an experienced Clinical Research Coordinator experience to support the day-to-day execution of clinical trials while also assisting with regulatory documentation and compliance activities.

This role coordinates participant visits, supports study enrollment, maintains regulatory documentation, and ensures clinical trials are conducted in accordance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

Candidates with experience as a Clinical Research Coordinator (CRC) or Clinical Trials Coordinator are strongly encouraged to apply.

What You Will Do

Clinical Trial Coordination

  • Screen potential research participants according to study eligibility criteria
  • Coordinate and schedule participant visits including screening, baseline, and follow-up visits
  • Guide participants through the informed consent process and answer study-related questions

Visit Preparation and Execution

  • Prepare charts, visit documentation, and study materials prior to participant visits
  • Coordinate day-of-visit workflow and ensure protocol procedures are completed

Clinical and Specimen Support

  • Perform or assist with specimen collection including blood draws
  • Process and document samples according to protocol requirements

Data and Documentation

  • Enter clinical study data into Electronic Data Capture (EDC) systems
  • Maintain accurate source documentation and respond to sponsor data queries

Regulatory Responsibilities

  • Maintain Investigator Site Files (ISF) and regulatory binders
  • Support IRB submissions, amendments, and continuing reviews
  • Maintain delegation logs, training documentation, and essential study documents
  • Track regulatory document expirations and investigator documentation
  • Support monitoring visits, audits, and regulatory inspections

Qualifications

Required

  • Bachelor's degree in life sciences, healthcare, public health, or related field, or equivalent clinical research experience
  • Minimum 2 years of clinical research experience as a Study Coordinator, Clinical Research Coordinator (CRC), or similar role
  • Knowledge of ICH-GCP guidelines
  • Experience using Electronic Data Capture (EDC) systems
  • Strong organizational and documentation skills
  • Phlebotomy or specimen collection experience

Preferred

  • Clinical research certification (CCRC or CCRP)
  • Experience maintaining regulatory binders or Investigator Site Files
  • Experience supporting IRB submissions

Compensation

Salary Range: $45,000 - $55,000 depending on experience

About Prime Clinical Research

Prime Clinical Research conducts clinical trials in partnership with pharmaceutical companies, biotechnology organizations, and contract research organizations. Our mission is to advance medical innovation while maintaining the highest standards of patient safety, regulatory compliance, and research quality.

Prime Clinical Research is an Equal Opportunity Employer.

Employment Type: FULL_TIME

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