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Trial Master File Jobs in Texas (NOW HIRING)

IQVIA Argentina

CRA 2, Oncology, IQVIA

Fort Worth, TX · On-site

$87.20 - $145.30/hr

Ensure copies or originals are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained per GCP and local regulations. * Create and ...

IQVIA

CRA 2, Oncology, IQVIA

Fort Worth, TX · On-site

$87K - $145K/yr

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...

IQVIA

CRA 2, Oncology, IQVIA

Dallas, TX

$87K - $145K/yr

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...

IQVIA

CRA 2, Oncology, IQVIA

Dallas, TX

$87K - $145K/yr

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...

IQVIA

CRA 2, Oncology, IQVIA

Houston, TX

$87K - $145K/yr

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...

IQVIA

CRA 2, Oncology, IQVIA

Fort Worth, TX

$87K - $145K/yr

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...

IQVIA

CRA 2, Oncology, IQVIA

San Antonio, TX

$87K - $145K/yr

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...

IQVIA

CRA 2, Oncology, IQVIA

San Antonio, TX · On-site

$87K - $145K/yr

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...

IQVIA

CRA 2, Oncology, IQVIA

Houston, TX · On-site

$87K - $145K/yr

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...

U.S. Renal Care

Clinical Research Coordinator

San Antonio, TX · On-site

$20.75 - $27.50/hr

Responsible for the preparation and ongoing maintenance of Essential Documents (The Trial Master File). This includes those documents that will allow for the evaluation of the clinical trial and ...

IQVIA

CRA 1, IQVIA Biotech

Houston, TX

$71K - $145K/yr

During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the ...

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How much do trial master file jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for trial master file in Texas is $34.93, according to ZipRecruiter salary data. Most workers in this role earn between $22.62 and $42.49 per hour, depending on experience, location, and employer.

What is a trial master file?

A Trial Master File (TMF) job involves managing and maintaining essential documents related to clinical trials to ensure compliance with regulatory requirements. Professionals in this role organize, track, and audit critical trial documentation to support inspections and submissions. They work closely with clinical teams, sponsors, and regulatory authorities to ensure proper documentation is accurate, complete, and audit-ready throughout the trial lifecycle.

What are the typical responsibilities and daily tasks of a trial master file specialist?

As a TMF Specialist, your main responsibilities include managing, organizing, and maintaining all essential clinical trial documentation to ensure compliance with regulatory standards. On a daily basis, you will review and upload documents to eTMF systems, track document status, resolve discrepancies, and support study teams during audits or inspections. You'll collaborate closely with clinical research associates, project managers, and quality assurance teams to ensure the TMF is complete and inspection-ready at all times. The work is detail-oriented and deadline-driven, offering opportunities to develop expertise in regulatory standards and advance into roles such as TMF Manager or Clinical Trial Associate.

What are the key skills and qualifications needed to thrive in the trial master file position, and why are they important?

To thrive in a Trial Master File (TMF) Specialist role, you need meticulous organizational skills, comprehensive knowledge of regulatory requirements for clinical trials, and often a bachelor's degree in life sciences or a related field. Familiarity with electronic Trial Master File (eTMF) systems, document management platforms, and relevant GCP (Good Clinical Practice) certifications is commonly required. Attention to detail, proactive communication, and the ability to collaborate effectively across clinical research teams are key soft skills. These competencies ensure regulatory compliance and seamless documentation, which are critical for the successful conduct and audit-readiness of clinical trials.

What are the most commonly searched types of Trial Master File jobs in Texas?

The most popular types of Trial Master File jobs in Texas are:

What are popular job titles related to Trial Master File jobs in Texas?

For Trial Master File jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Trial Master File jobs in Texas look for?

The top searched job categories for Trial Master File jobs in Texas are:

What cities in Texas are hiring for Trial Master File jobs?

Cities in Texas with the most Trial Master File job openings:

Trial Master File jobs near you
Infographic showing various Trial Master File job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 9% Part Time, 3% Contract, and 1% Nights. Highlights an 72% Physical, 2% Hybrid, and 26% Remote job distribution, with an average salary of $72,655 per year, or $34.9 per hour.

CRA 2, Oncology, IQVIA

Fort Worth, TX • On-site

IQVIA Argentina
See more jobs at IQVIA Argentinaexternal

$87.20 - $145.30/hr

Other

Posted 16 days ago

Job description

QA RA 2 – Clinical Research Associate

Fort Worth, United States of America | Full time | Field-based | R1537618

Essential Functions
  • Perform site monitoring visits (selection, initiation, monitoring, and close‑out) in accordance with contracted scope of work and regulatory requirements (Good Clinical Practice and International Conference on Harmonization guidelines).
  • Work with sites to adapt, drive, and track subject recruitment plans in line with project needs.
  • Administer protocol and study training to assigned sites and maintain regular communication to manage ongoing project expectations and issues.
  • Evaluate the quality and integrity of study site practices, ensuring proper protocol conduct and regulatory adherence; raise quality issues as appropriate.
  • Track study progress: regulatory submissions, approvals, recruitment, enrollment, case report form completion, and data query generation/resolution. May provide support during the start‑up phase.
  • Ensure copies or originals are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained per GCP and local regulations.
  • Create and maintain documentation for site management, monitoring visit findings, action plans, and other required study documentation.
  • Collaborate with study team members for project execution support as needed.
  • Manage site financial matters in accordance with the clinical trial agreement and retrieve invoices per local requirements where applicable.
Education & Experience
  • Bachelor’s degree (scientific discipline or health care preferred).
  • 1.5 to 2 years of relevant CRA experience, including on‑site monitoring.
Compensation

The potential base pay range for this role, when annualized, is $87,200.00 - $145,300.00. Actual base pay may vary based on qualifications, location, and schedule. Incentive plans, bonuses, and other benefits may be offered.

Equal Opportunity Employer

IQVIA is a proud equal‑opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other protected class.

Integrity Statement

IQVIA maintains a zero‑tolerance policy for candidate fraud. All application information and credentials must be truthful and complete. False statements or omissions will result in immediate disqualification or termination as appropriate.

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