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Clinical Monitoring Jobs in Texas (NOW HIRING)

Alira Health

Clinical Research Associate

Paris, TX

CRAs are highly motivated and function independently to conduct site monitoring responsibilities for clinical trials. CRAs work closely with the In-house CRAs, Lead CRAs, Director of Clinical ...

IQVIA

Senior Global Clinical Study Manager

Dallas, TX · On-site

Ensure clinical monitoring processes meet study needs and timelines * Partner with CRAs to optimize enrollment, data quality, and compliance Project & Stakeholder Management * Serve as primary client ...

IQVIA

Senior Global Clinical Study Manager

Dallas, TX · On-site

Ensure clinical monitoring processes meet study needs and timelines * Partner with CRAs to optimize enrollment, data quality, and compliance Project & Stakeholder Management * Serve as primary client ...

Cardinal Health

Clinical Pharmacist

Corpus Christi, TX · On-site

$114K - $136K/yr

Job Summary The Clinical Pharmacist assists with development of clinical programs, clinical monitoring, medication reconciliation, formulary management, cost containment programs, and improved ...

Cardinal Health

Clinical Pharmacist

Corpus Christi, TX · On-site

$114K - $136K/yr

Job Summary The Clinical Pharmacist assists with development of clinical programs, clinical monitoring, medication reconciliation, formulary management, cost containment programs, and improved ...

Cardinal Health, Inc.

Clinical Pharmacist

Corpus Christi, TX · On-site

$114K - $136K/yr

Job Summary The Clinical Pharmacist assists with development of clinical programs, clinical monitoring, medication reconciliation, formulary management, cost containment programs, and improved ...

Future Ventures

Clinical Research Associate

Austin, TX · On-site

$89 - $148/hr

Conduct site initiation, interim monitoring, and close‑out visits (remote and on‑site) * Ensure clinical studies are conducted in accordance with protocol, GCP, ISO 14155, and applicable ...

The Annex

Nurse Manager

Austin, TX · On-site

$95 - $130/hr

Administer medications, conduct health assessments, and perform clinical monitoring for residents in accordance with physician orders and The Annex's clinical protocols. * Complete all required ...

The Annex

Nurse Manager

Austin, TX · On-site

Administer medications, conduct health assessments, and perform clinical monitoring for residents in accordance with physician orders and The Annex's clinical protocols. * Complete all required ...

Soliant Health

Pharmacist | Ingram, Texas

Ingram, TX · On-site

$51 - $61.25/hr

Support decentralized pharmacy operations with interventions, patient counseling, and clinical monitoring * Ensure compliance with all regulatory and hospital policies Qualifications & Desired ...

AHS - Sherman Medical Center

Pharmacist PRN

Sherman, TX · On-site

$52 - $62.50/hr

The Pharmacist is responsible for the review and interpretation of physician orders, the dispensing of medications, the clinical monitoring of drug therapies and the provision of accurate and timely ...

AHS - Sherman Medical Center

Pharmacist -PRN

Sherman, TX · On-site

$52 - $62.50/hr

The Pharmacist is responsible for the review and interpretation of physician orders, the dispensing of medications, the clinical monitoring of drug therapies and the provision of accurate and timely ...

AHS Sherman Medical Center

Pharmacist -PRN

Sherman, TX · On-site

$52 - $62.50/hr

The Pharmacist is responsible for the review and interpretation of physician orders, the dispensing of medications, the clinical monitoring of drug therapies and the provision of accurate and timely ...

AHS - Sherman Medical Center

Pharmacist -PRN

Sherman, TX

$52 - $62.50/hr

The Pharmacist is responsible for the review and interpretation of physician orders, the dispensing of medications, the clinical monitoring of drug therapies and the provision of accurate and timely ...

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Showing results 21-40

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.

Clinical Research Associate

Alira Health

Paris, TX

Full-time

Re-posted 4 days ago

Key responsibilities

  • Conduct site monitoring visits including qualification, initiation, interim, and close-out visits, and document these visits properly.

  • Prepare monitoring visit reports that detail site-related issues, resolutions, protocol deviations, study progress, and enrollment status.

  • Ensure data integrity by reviewing source documents, reconciling adverse event reports, and verifying case report forms (CRFs).

Job description

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don't limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.

Job Description Summary

Job Description

ROLE

The Clinical Research Associate is an important member of the Alira Health Clinical team. CRAs are highly motivated and function independently to conduct site monitoring responsibilities for clinical trials. CRAs work closely with the In-house CRAs, Lead CRAs, Director of Clinical Monitoring and Project Managers to ensure sites' protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues.

KEY RESPONSABILITIES

  • Performs qualification, initiation, interim, and close-out visits and ensures proper documentation of site visits.

  • Prepares consistently accurate and timely monitoring visit reports documenting site-related problems, resolutions, actions taken, protocol deviations, study progress, and enrollment status.

  • Facilitates adverse event reporting and ensures the reconciliation of SAE reports with source documentation and CRFs.

  • Ensures integrity of CRF data through meticulous and thorough source document review and verification.

  • Conducts investigational product accountability.

  • Reviews regulatory binder for required documents.

  • Works closely with in-house CRAs and data management to resolve queries on discrepant data.

  • Proactively identifies site issues and develops problem-solving strategies for sites.

  • Maintains regular contact with study sites to ensure protocol/GCP compliance, assesses patient accrual rates, and responds to sponsor requests.

  • Conducts audit preparation at study sites as needed.

  • Works with other CRAs to maintain consistency and promote a collaborative team atmosphere.

  • Manages and resolves conflicting priorities to deliver on commitments.

  • Complies with ICH GCP guidelines, FDA regulations, and company SOPs.

  • Participates in industry and client meetings.

  • Performs additional duties as assigned.

DESIRED QUALIFICATION & EXPERIENCE

  • BS/BA from an undergraduate program or equivalent experience

  • 2 years of clinical research experience

TECHNICAL COMPETENCES & SOFT SKILLS

  • Ability to travel.

  • Proven ability to be careful, thorough, and detail-oriented.

  • Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment.

  • Self-starter who thrives in a collaborative, yet less structured team environment

  • Ability to problem-solve unstructured or ambiguous challenges.

  • Strong command of English, both written and verbal.

  • Excellent communication and interpersonal skills with customer service orientation.

  • Proficient with MS Office Suite, particularly Word and Excel.

  • Permanent authorization to work in the country where you are applying.

Languages

English

Education

Bachelor of Science (BS): Biology, Bachelor of Science (BS): Life Sciences

Contract Type

Regular

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