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Clinical Data Monitor Jobs in Texas (NOW HIRING)

Agilent

Clinical Affairs Scientist

Houston, TX · On-site +1

$105K - $197K/yr

Contribute to risk analyses, study quality control activities, and instream data monitoring in clinical trials. * Ensure scientific validity of reported results including statistical analysis ...

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Enter clinical data into Electronic Data Capture (EDC) systems. Maintain Trial Master File (TMF ... Prepare for monitoring visits, audits, and regulatory inspections. Ensure protocol compliance and ...

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Enter clinical data into Electronic Data Capture (EDC) systems. * Maintain Trial Master File (TMF ... Prepare for monitoring visits, audits, and regulatory inspections. * Ensure protocol compliance and ...

DM Clinical

Certified Medical Assistant (4063)

Irving, TX · On-site

$16.25 - $21/hr

Administer injections or vaccines, and monitor patients for adverse reactions. * Provide ... Perform regular audits on the clinical data to assess percent completeness and accuracy * Ensure ...

Driscoll

HEDIS Coordinator

Corpus Christi, TX · On-site

... monitor, and report quality initiatives and business processes which drive quality data capture ... Leads and collaborates in the project management of complex clinical data acquisition and ...

Icon plc

$91K - $114K/yr

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. * Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

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Clinical Data Monitor information

What is a clinical data monitor?

A Clinical Data Monitor is a professional responsible for overseeing the accuracy, integrity, and security of data collected during clinical trials. They ensure that clinical trial data is collected, entered, and reported according to regulatory standards and study protocols. Their work helps maintain the quality of data used to assess the safety and effectiveness of new drugs or medical devices. Clinical Data Monitors often collaborate with clinical research coordinators, data managers, and regulatory authorities to ensure compliance and resolve any data discrepancies.

How does a clinical data monitor typically interact with other teams during a clinical trial?

Clinical Data Monitors work closely with various teams such as clinical research associates (CRAs), data management, and biostatistics. They are responsible for ensuring the accuracy and integrity of clinical trial data by regularly reviewing case report forms and addressing discrepancies with site staff and data managers. Effective communication and collaboration are crucial, as Clinical Data Monitors often need to provide feedback, clarify data inconsistencies, and ensure all regulatory and protocol requirements are met throughout the trial.

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

To thrive as a Clinical Data Monitor, you need a solid understanding of clinical research processes, data management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and knowledge of Good Clinical Practice (GCP) guidelines are typically required. Attention to detail, analytical thinking, and strong communication skills set outstanding professionals apart in this role. These skills are crucial to ensure the accuracy, integrity, and regulatory compliance of clinical trial data, which supports successful drug development and patient safety.

What is the difference between Clinical Data Monitor vs Clinical Data Coordinator?

AspectClinical Data MonitorClinical Data Coordinator
CredentialsTypically requires a degree in life sciences or healthcare, often with certifications like CDMP or CDISCUsually holds a degree in health sciences or related field, with similar certifications
Work EnvironmentWorks primarily on data review, monitoring clinical trial sites, and ensuring data qualityHandles data entry, management, and coordination between sites and sponsors
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch organizations, hospitals, clinical trial sites

The Clinical Data Monitor focuses on reviewing and verifying clinical trial data to ensure accuracy and compliance, often working directly with sites. The Clinical Data Coordinator manages data entry and organization, supporting the data collection process. Both roles require similar educational backgrounds and certifications but differ in daily responsibilities and focus areas.

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

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

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

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

Clinical Data Monitor jobs near you
Infographic showing various Clinical Data Monitor job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 10% Part Time, and 2% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution.

Clinical Affairs Scientist

Agilent

Houston, TX • On-site, Remote

$105K - $197K/yr

Full-time

Posted 16 days ago

Key responsibilities

  • Support clinical trial study designs and execution, including authoring study protocols and reports.

  • Collaborate with cross-functional teams and external partners to generate clinical evidence and ensure compliance.

  • Provide scientific oversight and contribute to regulatory submissions, scientific publications, and presentations.

Agilent Technologies rating

8.5

Company rating: 8.5 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

33rd of 545 rated manufacturers

Job description

Job Description

We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical diagnostic field as a key member of the Organization of Chief Medical Officer(OCMO) Global Clinical Affairs team. The CAS' main responsibilities will be to support clinical evidence generation, in conjunction with cross-functional teams as part of the co-development process of companion diagnostics in the field of oncology. This position will support clinical trial study designs and execution, regulatory applications, and scientific marketing deliverables. The ideal candidate will have a strong background in clinical science/research and experience working in pharmaceutical, biomarker, and/or in vitro diagnostic clinical development. The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and external requirements. This position reports to the Manager of Clinical Affairs Sciences and has no direct reports.
Responsibilities include but are not limited to:

  • Provide thought leadership on key relevant clinical topics to support strategy development and execution.

  • Generation of content to support external validation studies including study design and authoring of study protocols and reports. May also contribute to cutoff/cutpoint determination studies, method comparison, bridging, and analytical concordance studies.

  • Design and develop databases, Electronic Data Capture (EDC) systems, and case report forms.

  • Contribute to risk analyses, study quality control activities, and instream data monitoring in clinical trials.

  • Ensure scientific validity of reported results including statistical analysis, tabulation, and presentation of data.

  • Collaborate with regulatory and development teams during the submission process including authoring of clinical performance information and other documentation such as Instructions for Use (IFU).

  • Provide clinical and scientific oversight of local marketing and commercial materials.

  • Ensure effective, efficient and compliant Clinical Affairs processes including preparing, revising, and maintaining standard operating procedures for the conduct of clinical studies.

  • Serve as the clinical science subject matter expert in cross-functional internal meetings as well as meetings with pharmaceutical partners and regulatory bodies.

  • Author manuscripts, abstracts, whitepapers and prepare oral/poster presentations.

  • Support audits and inspections as a clinical subject matter expert.

Qualifications

  • Master's degree or advanced degree (e.g., Ph.D., Pharm. D., M.D.) in pharmaceutical, medical or relevant biomedical science fields. Advanced Degree preferred.

  • 4+ years of experience in IVD product development, clinical research, medical writing, and/or clinical science in the medical device and/or pharmaceutical industry.

  • Familiarity with clinical trial design, conduct, and oversight including biostatistics, and Good Clinical Practice preferred.

  • Ability to interpret regulatory standards, guidance, and laws.

  • Strong scientific, medical writing, and presentation skills

  • Exceptional ability to manage multiple projects in a fast-paced environment with changing priorities.

  • Must be able to work and make independent decisions, understand complex scientific and clinical data information, and be able to take the initiative to lead projects and assignments.

  • Experience working with external partners and/or regulatory bodies including the FDA.

  • Knowledge in oncology, immunology, and/or pathology preferred.

Additional Details

This job has a full time weekly schedule. It includes the option to work remotely. Applications for this job will be accepted until at least August 27, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $105,280.00 - $197,400.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required: NoShift: DayDuration: No End DateJob Function: Medical/Clinical

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