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Clinical Monitoring Jobs in Texas (NOW HIRING)

Adams Clinical

Lead Dosing Session Monitor

Dallas, TX · On-site

$60 - $70/hr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... These include pre-dose preparation, real-time monitoring during psychedelic dosing sessions, and ...

Adams Clinical

Lead Dosing Session Monitor

Dallas, TX · On-site

$60 - $70/hr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... These include pre-dose preparation, real-time monitoring during psychedelic dosing sessions, and ...

Adams Clinical

Lead Dosing Session Monitor

Dallas, TX

$60 - $70/hr

Join Us in Shaping the Future of Clinical Research   Adams Clinical is a leading clinical trial ... These include pre-dose preparation, real-time monitoring during psychedelic dosing sessions, and ...

Clinical Research Solution LLC

Be Seen First

Clinical Study Coordinator

Houston, TX · On-site

$49K - $59K/yr

Position Summary The Clinical Research Coordinator will support daily clinical trial operations ... Communicate with sponsors/CROs regarding queries and monitoring visits * Assist with regulatory ...

Adams Clinical

Clinical Research Assistant

Desoto, TX

$19.23 - $23.08/hr

Support CRCs during monitoring visits and assist with preparing documentation and materials to ... Basic understanding of clinical research principles is a plus. * Strong attention to detail ...

Adams Clinical

Clinical Research Assistant

Desoto, TX

$19.23 - $23.08/hr

Support CRCs during monitoring visits and assist with preparing documentation and materials to ... Basic understanding of clinical research principles is a plus. * Strong attention to detail ...

Adams Clinical

Clinical Research Assistant

Desoto, TX · On-site

$19.23 - $23.08/hr

Support CRCs during monitoring visits and assist with preparing documentation and materials to ... Basic understanding of clinical research principles is a plus. * Strong attention to detail ...

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All JobsClinical Monitoring JobsClinical Monitoring Jobs in Texas

Clinical Monitoring information

See Texas salary details

$11

$38

$64

How much do clinical monitoring jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical monitoring in Texas is $38.31, according to ZipRecruiter salary data. Most workers in this role earn between $26.88 and $49.04 per hour, depending on experience, location, and employer.

What is clinical monitoring?

Clinical monitoring is the process of overseeing clinical trials to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures, Good Clinical Practice (GCP), and regulatory requirements. Clinical monitors, often called Clinical Research Associates (CRAs), are responsible for checking the progress of a clinical trial at research sites, verifying data accuracy, ensuring participant safety, and ensuring compliance with regulations. Their work is essential in maintaining the integrity of clinical data and the safety of trial participants.

What are the key skills and qualifications needed to thrive in clinical monitoring, and why are they important?

To thrive in Clinical Monitoring, you need a solid background in life sciences or nursing, strong knowledge of clinical trial protocols, and often a relevant degree such as a BS in a scientific field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and certifications like ACRP or SOCRA are highly valued. Exceptional attention to detail, strong organizational skills, and effective communication are crucial soft skills for managing trial sites and ensuring compliance. These competencies are vital for ensuring data integrity, regulatory adherence, and the smooth progress of clinical trials.

What are some common challenges faced by professionals in clinical monitoring, and how can they be addressed?

Clinical Monitoring professionals often encounter challenges such as managing multiple study sites, ensuring protocol compliance, and maintaining clear communication with site staff. Navigating regulatory requirements and handling unexpected issues, like protocol deviations or data discrepancies, can also be demanding. To address these, strong organizational skills, proactive communication, and thorough documentation are essential. Building collaborative relationships with site personnel and staying updated on regulatory guidelines can help ensure smoother study progress and data integrity.

What is the difference between Clinical Monitoring vs Clinical Data Management?

AspectClinical MonitoringClinical Data Management
Primary RoleOversees site activities, ensures protocol adherence, monitors patient safetyCollects, validates, and manages clinical trial data
Required CredentialsTypically a degree in life sciences, nursing, or related field; often requires monitoring certificationsDegree in life sciences, biostatistics, or related; data management certifications beneficial
Work EnvironmentOn-site at clinical trial sites or remotely, interacting with site staffPrimarily office-based, working with electronic data capture systems
Industry UsageCommonly used in clinical trial phases, especially during site visitsUsed throughout the trial for data collection, cleaning, and analysis

Clinical Monitoring focuses on overseeing clinical trial sites and ensuring compliance, while Clinical Data Management handles the collection and validation of trial data. Both roles are essential in clinical research, often working closely but with distinct responsibilities.

What are popular job titles related to Clinical Monitoring jobs in Texas?

For Clinical Monitoring jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Clinical Monitoring jobs in Texas look for?

The top searched job categories for Clinical Monitoring jobs in Texas are:

What cities in Texas are hiring for Clinical Monitoring jobs?

Cities in Texas with the most Clinical Monitoring job openings:

Clinical Monitoring jobs near you
Infographic showing various Clinical Monitoring job openings in Texas as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $79,695 per year, or $38.3 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