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Clinical Trials Associate Jobs in Texas (NOW HIRING)

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$91K - $114K/yr

Clinical Research Associate - West Coast ICON is a global healthcare intelligence and clinical ... As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data ...

Immatics NV

Senior Clinical Research Associate

Houston, TX · On-site

$120K - $135K/yr

Associate Director, Team Lead Site Operations Location :FullyRemote Salary Range: $120,000 to $135 ... Experience in oncology clinical trials or related therapeutic areas * Advanced presentation ...

Socket.dev

Clinical Research Coordinator II

Lewisville, TX · On-site

$60 - $95/hr

The CRC II is responsible for coordinating and managing clinical trials designed to test the ... Associate's degree in healthcare or related field preferred. * Minimum of 4 years of experience in ...

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MD Anderson

Clinical Trial Technician

Houston, TX

$26.44 - $31.73/hr

We strive to provide outstanding patient care while performing innovative Phase 1 trials with new ... Associate's Degree in Public Health, Healthcare Administration, or a related scientific field ...

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How much do clinical trials associate jobs pay per hour?

As of Sep 2, 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:

Clinical Trials Associate jobs near you
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.

Senior Clinical Research Coordinator

ALLIANCE CLINICAL LLC

Lewisville, TX • On-site

$65 - $95/hr

Other

Posted 12 days ago

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Senior Clinical Research Coordinator

Alliance Clinical Lewisville, Lewisville, TX, US

11 days ago Requisition ID: 1336

Summary:

The Senior Clinical Research Coordinator (Senior CRC) oversees the planning and management of study projects, ensuring compliance with protocols and regulatory requirements. This role coordinates the study activities, manages data collection, and supports investigators with reporting and documentation. The Senior CRC plays a critical role in maintaining the integrity and efficiency of research operations.

Essential Duties and Responsibilities:

  • Provide work directions to clinical staff and back-office team.
  • Provide operational leadership to resolve complex study and site-level issues impacting enrollment, compliance, and timelines.
  • Review, comprehend, and communicate study protocols.
  • Oversee SIV, PSV and IMV.
  • Assist CRC team as needed to facilitate research and business needs.
  • Conduct and manage clinical trials in accordance with the study protocol guidelines and internal SOPs.
  • Oversee data quality and ensure accuracy and timelines of study data across assigned protocols.
  • Work closely with CRO/CRA and IRB.
  • Manage required study start up documentation, training, and timelines on assigned study protocols
  • Effectively communicate with sponsors, ensuring customer satisfaction.
  • Direct study resource planning and ensure appropriate allocation of supplies and equipment.
  • Perform other duties as assigned.

Qualifications:

  • Associate's degree and/or completion of accredited healthcare certification program.
  • Ability to effectively lead, coach and direct employees.
  • Strong leadership skills that empower an engaged and effective team.
  • Exceptional communication skills, including verbal and written communication.
  • Ability to prioritize critical tasks and effectively manage time.
  • Minimum of 2 years of experience in clinical research.
  • Minimum of 2 years of experience working as a Clinical Research Coordinator preferred.
  • Comprehensive knowledge of FDA, GCP & confidentiality.
  • Exceptional attention to detail and strong organizational skills.
  • Proven ability to multi-task in a rapidly changing environment.
  • High emotional intelligence, with the ability to identify and effectively control stressful situations.

ACN does not provide visa sponsorship for this role. Candidates who will require immigration or visa sponsorship at any time now or in the future (including, but not limited to, H-1B, TN, or STEM OPT training plans) are not eligible for this role.

About the Company:

At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.

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