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Clinical Trials Associate Jobs in Texas (NOW HIRING)

As a Clinical Research Associate, you'll play a crucial role in pioneering groundbreaking clinical ... Your work will directly contribute to the planning, execution, and success of innovative trials ...

Clinical Trial Technician

Houston, TX · On-site

$26.44 - $31.73/hr

This role provides valuable exposure to clinical trials, laboratory operations, regulatory ... Associate's Degree in Public Health, Healthcare Administration, or a related scientific field • ...

This role provides valuable exposure to clinical trials, laboratory operations, regulatory ... Associate's Degree in Public Health, Healthcare Administration, or a related scientific field • ...

Clinical Trial Technician

Houston, TX · On-site

$26.44 - $31.73/hr

This role provides valuable exposure to clinical trials, laboratory operations, regulatory ... Associate's Degree in Public Health, Healthcare Administration, or a related scientific field • ...

These include FDAregulated clinical trials involving investigational drugs and medical devices ... Education High School Diploma or Associate's Degree in medical or science related field or Bachelor ...

Clinical Research Coordinator II

Lubbock, TX · On-site

$20.75 - $27.75/hr

Independently coordinate and manage industry-sponsored clinical trials from study start-up through ... Associate's or Bachelor's degree in a scientific, healthcare, or related discipline required * 3-5 ...

Clinical Research Coordinator II

Plano, TX · On-site

$23.25 - $30.75/hr

Independently coordinate and manage industry-sponsored clinical trials from study start-up through ... Associate's or Bachelor's degree in a scientific, healthcare, or related discipline required * 3-5 ...

Showing results 41-60

Clinical Trials Associate information

See Texas salary details

$16

$37

$65

How much do clinical trials associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical trials associate in Texas is $37.25, according to ZipRecruiter salary data. Most workers in this role earn between $30.00 and $40.96 per hour, depending on experience, location, and employer.

What is a clinical trials associate?

Clinical Trials Associates (CTAs) are professionals who support the planning, coordination, and administration of clinical research studies, often working under the supervision of Clinical Research Coordinators or Managers. Their responsibilities typically include maintaining study documentation, ensuring regulatory compliance, assisting with data collection, and communicating with study sites. CTAs play a critical role in ensuring that clinical trials run smoothly and adhere to strict protocols and guidelines. Their work helps bring new medical treatments and therapies to market safely and efficiently.

What are the key skills and qualifications needed to thrive as a clinical trials associate, and why are they important?

To thrive as a Clinical Trials Associate, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, typically supported by a life sciences degree. Familiarity with systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and knowledge of Good Clinical Practice (GCP) guidelines or related certifications is important. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating study activities and collaborating with diverse teams. These skills ensure accurate trial execution, regulatory adherence, and successful study outcomes.

What are some common challenges faced by clinical trials associates, and how can they be managed effectively?

Clinical Trials Associates often face challenges such as coordinating with multiple stakeholders, managing tight deadlines, and ensuring strict compliance with regulatory guidelines. Balancing administrative tasks with participant communication requires strong organizational skills and attention to detail. Staying proactive in communication, utilizing project management tools, and seeking guidance from senior team members can help manage these challenges effectively while fostering a collaborative team environment.

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

AspectClinical Trials AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRA are commonBachelor's degree in health sciences or related field; certifications like CCRP are advantageous
Work EnvironmentTypically works in clinical trial sites, pharmaceutical companies, or CROsWorks directly at clinical sites, hospitals, or research centers
Job FocusSupports trial setup, data entry, and regulatory complianceManages patient recruitment, scheduling, and data collection

While both roles support clinical research, Clinical Trials Associates primarily focus on trial logistics and compliance, whereas Clinical Research Coordinators handle patient interactions and site management. Both positions require similar educational backgrounds and certifications, often working in the same environments, but their daily responsibilities differ.

Is a clinical trials associate a good career?

A clinical trials associate is a valuable role in the healthcare and pharmaceutical industries, responsible for coordinating and monitoring clinical trial activities. It offers opportunities for career growth, requires attention to detail, and often involves working with regulatory guidelines and data management tools. The role can be stable and rewarding for those interested in medical research and patient safety.

What do I need to be a clinical trials associate?

To become a clinical trials associate, candidates typically need a bachelor's degree in life sciences, healthcare, or a related field. Relevant skills include knowledge of Good Clinical Practice (GCP), attention to detail, and experience with clinical trial management systems or regulatory documentation. Certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.

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

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

What cities in Texas are hiring for Clinical Trials Associate jobs?

Cities in Texas with the most Clinical Trials Associate job openings:

Infographic showing various Clinical Trials Associate 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 $77,485 per year, or $37.3 per hour.

Assoc/Full Professor - Division Chief, Hematology & Oncology

The Chronicle Of Higher Education, Inc.

Lubbock, TX • On-site

Other

Re-posted 22 days ago


Job description

Position Title

Assoc/Full Professor – Division Chief, Hematology & Oncology

Position Summary

Texas Tech University Health Sciences Center seeks an outstanding physician‑leader to serve as Chief of the Division of Hematology & Oncology and Medical Director of the University Medical Center TLC² Foundation Cancer Center. The role involves strategic, clinical, academic and operational leadership for the division, the cancer center and affiliated service lines.

Career‑Defining Opportunity

The new 124,000‑sq‑ft comprehensive academic cancer center opened on April 20, 2026. It offers advanced radiation oncology, infusion and chemotherapy services, outpatient adult and pediatric oncology clinics, dedicated infusion and specialty pharmacies, research space and clinical trials (Phase I‑III), as well as integrative medicine services.

Major/Essential Functions
  • Provide strategic, clinical, academic, and operational leadership for the Division, the Center, and the service line.
  • Continue development of a premier multidisciplinary oncology program recognized regionally.
  • Direct multi‑disciplinary clinical services, spanning pediatric through adult, inclusive of surgery, radiation oncology, palliative care, and additional subspecialties, toward a team‑oriented, patient‑focused program.
  • Increase clinical trials (Phase I–III) and strengthen collaborations with NCI, DoD, CPRIT‑funded researchers, cooperative groups, and industry‑sponsored trials.
  • Advance academic scholarship efforts while increasing extramural funding.
  • Retain, recruit, mentor, and develop Hematology/Oncology faculty.
  • Advise and provide oversight of the Hematology/Oncology Fellowship Program.
  • Lead a practitioner, engage in direct patient care through ongoing clinical practice, inclusive of supervision and teaching.
Preferred Qualifications
  • 5+ years of clinical leadership experience.
  • 5+ years of research experience.
  • Demonstrated success in clinical trials.
  • Demonstrated success in scholarship.
  • Demonstrated success in extramural funding.
Required Qualifications
  • MD or DO.
  • ABMS Board Certified in Internal Medicine.
  • ABMS Board Certified in Hematology & Oncology.
  • 5+ years of clinical practice.
  • 2+ years of clinical leadership experience.
Other Job Details
  • Pay: Salary commensurate with related education, experience, and skills.
  • Pay Basis: Monthly.
  • Work Location: Lubbock.
  • Job Type: Full Time.
  • Travel: Up to 25%.
  • Requisition ID: 44866BR.
EEO Statement

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, genetic information or status as a protected veteran.

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