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Clinical Study Associate Jobs in Texas (NOW HIRING)

DM Clinical

Study Manager I (4011)

Sugar Land, 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 ...

Becton, Dickinson and Company

Study & Site Management * Serve as CRA for assigned complex clinical studies, providing expert ... associates through our comprehensive Total Rewards program. We are committed to attracting and ...

DiaSorin

Clinical Research Associate

Austin, TX · On-site

Job Scope The Clinicial Research Associate will be responsible for conducting day-to-day work ... Create clinical study document designs and tracking tools. * Investigate queries, monitor ...

DiaSorin

Clinical Research Associate

Austin, TX

Job Scope The Clinicial Research Associate will be responsible for conducting day-to-day work ... Create clinical study document designs and tracking tools. * Investigate queries, monitor ...

Icon plc

$91K - $114K/yr

Clinical Research Associate - West Coast ICON is a global healthcare intelligence and clinical ... Contributing to the preparation and review of study documentation, including protocols and clinical ...

Arkray Group

Regulatory Affairs Associate

Plano, TX · On-site

$60 - $80/hr

Travel to clinical study sites for setup, training, monitoring, and other study support as needed. * Perform in-house evaluative/bench studies of ARKRAY products, new products, and competitive ...

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Clinical Study Associate information

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How much do clinical study associate jobs pay per hour?

As of Sep 7, 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 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 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 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 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, 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 $61,120 per year, or $29.4 per hour.

Associate Clinical Study Manager

Worldwide Clinical Trials

San Antonio, TX • On-site

Other

Posted 18 days ago

Job description

What the Associate Clinical Study Manager does at Worldwide


The Associate, Clinical Study Manager will be responsible for the site-level monitoring activities of on one or more allocated Phase I through IV Clinical Trials that may be local, regional, or global in scope. Supports the CSM with directing the technical, financial, and operational aspects to ensure the successful completion of the clinical trials. Works with functional area leads to identify and evaluate essential project prerequisites. The ACSM cooperates with the CSM to ensure all project deliverables meet client’s time/quality/cost expectations.


What you will do


  • Coordinate study monitoring visits, to include (but not limited to): ensuring the monitor has access to the relevant electronic systems, reserving monitoring space, assembling study documents for CRA review, and ensuring all follow-up action items are completed in a timely manner.
  • Work collaboratively with other clinic departments to ensure all queries are answered in a timely manner.
  • Manage and store signed approval forms for Clinical Lab, PK processing, Clinspark Go live, and Clinspark training and access request forms from clients.
  • Coordinate and collate signature forms for SIV attendance, logistics meetings, and any other protocol training related meetings, file in the appropriate study folder.
  • Ensure staff training is documented in the appropriate study files on the study protocol and other related processes, adhere to professional standards and to SOPs as well as current Good Clinical Practice (GCP) and applicable local regulations.
  • Facilitate shipment of samples to bioanalytical labs for analysis per the study timeline and/or client request.


What you will bring to the role


  • Excellent communication, planning, and organizational skills.
  • Sense of urgency and ability to be adaptable in a fast-paced and rapidly changing environment.
  • Self-motivated and excellent problem-solving skills.
  • Ability to work independently.
  • Ability to negotiate and liaise with clients in a professional manner.
  • Must have satisfactory customer service skills.


Your experience


  • Bachelor’s Degree (Life Sciences or Health preferred) or 4 years clinical research experience Or Associates Degree with 2 years clinical research experience.
  • Min 1 year as a Clinical Research Coordinator preferred


Apply