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Trial Master File Manager Jobs in Texas (NOW HIRING)

IQVIA

CRA 1, IQVIA Biotech

Dallas, TX

$71K - $145K/yr

... site management activities. In this position, you will ensure that assigned study sites conduct ... the Trial Master File (TMF) and the Investigator Site File (ISF). A central part of this role ...

IQVIA

CRA 1, IQVIA Biotech

Fort Worth, TX

$71K - $145K/yr

... site management activities. In this position, you will ensure that assigned study sites conduct ... the Trial Master File (TMF) and the Investigator Site File (ISF). A central part of this role ...

IQVIA

CRA 1, IQVIA Biotech

Dallas, TX

$71K - $145K/yr

... site management activities. In this position, you will ensure that assigned study sites conduct ... the Trial Master File (TMF) and the Investigator Site File (ISF). A central part of this role ...

IQVIA

CRA 1, IQVIA Biotech

San Antonio, TX

$71K - $145K/yr

... site management activities. In this position, you will ensure that assigned study sites conduct ... the Trial Master File (TMF) and the Investigator Site File (ISF). A central part of this role ...

SGS

Quality Assurance Specialist

Richardson, TX · On-site

Conducts audits of clinical trial master files, source data, and procedures for protocol ... Other duties or tasks assigned by manager * Work with all involved parties to ensure that both the ...

State Farm

Trial Attorney

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

File ownership * Effective written and oral communication skills Technology/software experience ... Working knowledge of a Case Management system * Working Knowledge of a Document Storage system ...

NACBA

Trial Attorney

San Antonio, TX · On-site

$117.50 - $170/hr

  • Medical

  • Dental

  • Vision

  • Retirement

Location US-TX-San Antonio Job Category Legal, Compliance, and Risk Management Position Type ... File ownership * Effective written and oral communication skills Technology/software experience ...

State Farm

Trial Attorney

Houston, TX · Hybrid

  • Medical

  • Dental

  • Vision

  • Retirement

File ownership * Effective written and oral communication skills Technology/software experience ... Working knowledge of a Case Management system * Working Knowledge of a Document Storage system ...

State Farm

Trial Attorney

San Antonio, TX · Hybrid

  • Medical

  • Dental

  • Vision

  • Retirement

File ownership * Effective written and oral communication skills Technology/software experience ... Working knowledge of a Case Management system * Working Knowledge of a Document Storage system ...

State Farm

Trial Attorney

San Antonio, TX · On-site

$117.50 - $170/hr

  • Medical

  • Dental

  • Vision

  • Retirement

File ownership * Effective written and oral communication skills Technology/software experience ... Working knowledge of a Case Management system * Working Knowledge of a Document Storage system ...

Nationwide

Senior Trial Attorney

Houston, TX · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... management systems, and electronic filing procedures. * Commitment to the highest standards of ... Nationwide Trial Division is a national team with approximately 40 offices through six regions ...

State Farm

Trial Attorney

San Antonio, TX · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

File ownership * Effective written and oral communication skills Technology/software experience ... Working knowledge of a Case Management system * Working Knowledge of a Document Storage system ...

Veterinary Pet Insurance

Senior Trial Attorney

San Antonio, TX · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... management systems, and electronic filing procedures. * Commitment to the highest standards of ... Nationwide Trial Division is a national team with approximately 40 offices through six regions ...

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Showing results 41-60

All JobsTrial Master File JobsTrial Master File Manager JobsTrial Master File Manager Jobs in Texas

Trial Master File Manager information

See Texas salary details

$41.5K

$70.4K

$106.2K

How much do trial master file manager jobs pay per year?

As of Aug 15, 2026, the average yearly pay for trial master file manager in Texas is $70,418.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,700.00 and $87,100.00 per year, depending on experience, location, and employer.

What are some common challenges faced by trial master file managers, and how can they be addressed?

Trial Master File Managers often encounter challenges such as ensuring TMF completeness, maintaining regulatory compliance, and coordinating document submissions across multiple stakeholders. Keeping documents up-to-date and audit-ready requires strong attention to detail and effective communication with clinical teams, vendors, and sponsors. Leveraging electronic TMF systems, implementing standardized processes, and promoting regular training can help address these challenges and ensure the integrity of the TMF throughout a study.

What is a trial master file manager?

A Trial Master File Manager is a professional responsible for overseeing the creation, maintenance, and quality control of the Trial Master File (TMF) in clinical research. The TMF is a collection of essential documents that allow the conduct of a clinical trial to be reconstructed and evaluated. The manager ensures that all documents are complete, accurate, and compliant with regulatory requirements throughout the trial's lifecycle. They work closely with clinical teams, auditors, and regulatory authorities to guarantee readiness for inspections and audits. Their role is crucial for maintaining transparency and credibility in clinical research processes.

What are the key skills and qualifications needed to thrive as a trial master file manager?

To thrive as a Trial Master File Manager, you typically need a strong background in clinical research, regulatory requirements, and document management, often supported by a degree in life sciences or a related field. Familiarity with electronic Trial Master File (eTMF) systems, GCP guidelines, and relevant industry certifications like DIA's TMF Professional Certification is important. Attention to detail, organizational skills, and effective communication help ensure TMF integrity and coordination across cross-functional teams. These skills are crucial for maintaining regulatory compliance, audit readiness, and efficient clinical trial operations.

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 Manager jobs in Texas?

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

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

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

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

Trial Master File Manager jobs near you

CRA 1, IQVIA Biotech

IQVIA

Dallas, TX

$71K - $145K/yr

Full-time

Re-posted yesterday

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 rated it services

Job description

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring in oncology solid tumor.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Job Overview

The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities. In this position, you will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical Practice (GCP), and ICH guidelines. This role is essential in protecting patient safety, ensuring highquality clinical data, and maintaining study integrity.

Key Responsibilities

As a CRA I, you will conduct various types of monitoring visits-including site selection, initiation, routine monitoring, and closeout visits-to evaluate the quality and integrity of site practices. You will verify that study activities are performed according to regulatory requirements and sponsor expectations, escalating quality concerns as necessary. 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 Investigator Site File (ISF).

A central part of this role involves building and maintaining strong communication with investigative sites. You will provide protocol training, set expectations, address sitelevel challenges, and support recruitment planning to help sites meet enrollment targets. You will also collaborate closely with internal project teams to ensure cohesive study execution and may contribute to site-level financial processes or startup activities based on study needs.

Accurate and timely documentation is critical. The CRA I prepare detailed monitoring visit reports, followup letters, and all required study documentation to ensure audit readiness and transparent oversight. The ability to manage multiple tasks, prioritize effectively, and work independently while maintaining productive team relationships is essential for success.

Qualifications

  • Bachelor's degree required; a scientific or healthcare discipline is preferred.
  • 6 months -2 years of relevant experience, with equivalent combinations of education, training, or completion of a CRA training program considered.
  • Basic knowledge of clinical research regulations (GCP/ICH).
  • Ability to travel as required by the project.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an 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 status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $71,900.00 - $145,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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