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Clinical Study Associate Jobs in Texas (NOW HIRING)

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 ...

Neuralink

Clinical Research Associate

Austin, TX · On-site

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

Neuralink

Clinical Research Associate

Austin, TX · On-site

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

MSD

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

New

Neuralink

Clinical Research Associate

Austin, TX · On-site

$89K - $148K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

As a Clinical Research Associate, you'll play a crucial role in pioneering groundbreaking clinical ... Ensure clinical studies are conducted in accordance with protocol, GCP, ISO 14155, and applicable ...

Abbott

Clinical Contracts Associate II

Plano, TX · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Clinical Contract Associatepositionwith Sylmar, CA, Santa Clara, CA, Plano, TXor Maple Grove, MN as ... Servesas a Business Unit champion/core team member/single point of contact for all study contract ...

Abbott

Clinical Contracts Associate II

Plano, TX

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Clinical Contract Associatepositionwith Sylmar, CA, Santa Clara, CA, Plano, TXor Maple Grove, MN as ... Servesas a Business Unit champion/core team member/single point of contact for all study contract ...

Merck & Co.

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

Merck & Co.

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

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Showing results 21-40

All JobsClinical Study Associate JobsClinical Study Associate Jobs in Texas

Clinical Study Associate information

See Texas salary details

$11

$29

$51

How much do clinical study associate jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for clinical study associate in Texas is $29.38, according to ZipRecruiter salary data. Most workers in this role earn between $19.71 and $38.75 per hour, depending on experience, location, and employer.

What is a clinical study associate?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

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

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

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

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What are some common challenges clinical study associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.

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 Associate jobs?

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

Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in Texas as of August 2026, with employment types broken down into 2% As Needed, 77% Full Time, 15% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $61,120 per year, or $29.4 per hour.

Clinical Research Accounts Billing Specialist

Salma Mazhar MD PA

Mesquite, TX • On-site

Part-time

Re-posted 11 days ago

Job description

 Summary:

The Clinical Research Accounts Billing Specialist is responsible for managing the financial and billing activities related to clinical trials. This role ensures accurate invoicing, payment tracking, and compliance with study budgets, contracts, and sponsor requirements. The specialist works closely with clinical operations, sponsors, and finance teams to ensure timely and accurate revenue cycle management. THIS IS A PART TIME OPPORTUNITY.
Key Responsibilities:

  •  Prepare, review, and submit invoices to sponsors and CROs based on clinical trial agreements and milestones 
  •  Reconcile study budgets with completed patient visits, procedures, and data entries (e.g., EDC systems) 
  •  Track accounts receivable and follow up on outstanding payments 
  •  Resolve billing discrepancies, denials, and payment variances 
  •  Maintain accurate financial records for each clinical study 
  •  Collaborate with study coordinators and project managers to verify subject visits and billable events 
  •  Ensure compliance with contracts, protocols, and regulatory requirements 
  •  Assist in budget development and coverage analysis when needed 
  •  Generate financial reports for management (aging reports, revenue tracking, etc.) 
  •  Support audits by providing required billing documentation 
Required Qualifications:

  •  Associate’s or Bachelor’s degree in Accounting, Finance, Healthcare Administration, or related field 
  •  2+ years of experience in medical billing, clinical research billing, or healthcare finance 
  •  Strong understanding of clinical trial billing processes and sponsor invoicing 
  •  Experience with CRIO or other CTMS preferred 
  •  Proficiency in Microsoft Excel and accounting software 
  •  High attention to detail and strong organizational skills 
Preferred Qualifications:

  •  Experience working in a clinical research site, CRO, or sponsor environment 
  •  Knowledge of clinical trial agreements, budgets, and coverage analysis 
  •  Familiarity with Medicare billing rules related to clinical trials 
  •  Certification in clinical research (e.g., ACRP, SOCRA) is a plus 
Key Skills:

  •  Analytical and problem-solving skills 
  •  Strong communication and follow-up abilities 
  •  Time management and multitasking 
  •  Financial reconciliation and reporting 
  •  Knowledge of regulatory compliance in clinical research 
Work Environment:

  •  OFFICE BASED. Remote is not available.
  •  May require coordination with multiple departments and external sponsors