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Temp Trial Master File Specialist Jobs (NOW HIRING)

Manage Trial Master File (TMF) documentation. * Coordinate study working groups and stakeholder meetings. * Ensure ClinicalTrials.gov registration and reporting requirements are met. * Monitor study ...

Spec 3, Clinical Research

Irvine, CA · On-site

  • Medical

  • Life

  • Retirement

... Specialist supports all phases of clinical studies, including study start-up, conduct, and closeout, with a primary focus on maintaining an audit- and inspection-ready Trial Master File (TMF). This ...

Clinical Trial Manager

Frederick, MD · On-site

$125K - $143K/yr

Manage Trial Master File (TMF) documentation. * Coordinate study working groups and stakeholder meetings. * Ensure ClinicalTrials.gov registration and reporting requirements are met. * Monitor study ...

Clinical Trial Manager

Berkeley, CA · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Maintain and oversee the Trial Master File (TMF), ensuring completeness, quality, and continuous inspection readiness * Review and/or approve site-specific documents, including informed consent forms ...

Clinical Trial Manager

Berkeley, CA · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Maintain and oversee the Trial Master File (TMF), ensuring completeness, quality, and continuous inspection readiness * Review and/or approve site-specific documents, including informed consent forms ...

... Trial Master File. It's the evidence base regulators, auditors, and inspectors turn to when they ... In parallel, you'll work regularly with the Study File Specialists working across studies. Cross ...

... Trial Master File. It's the evidence base regulators, auditors, and inspectors turn to when they ... In parallel, you'll work regularly with the Study File Specialists working across studies. Cross ...

... Trial Master File. It's the evidence base regulators, auditors, and inspectors turn to when they ... In parallel, you'll work regularly with the Study File Specialists working across studies. Cross ...

... Trial Master File. It's the evidence base regulators, auditors, and inspectors turn to when they ... In parallel, you'll work regularly with the Study File Specialists working across studies. Cross ...

... Trial Master File. It's the evidence base regulators, auditors, and inspectors turn to when they ... In parallel, you'll work regularly with the Study File Specialists working across studies. Cross ...

Senior Clinical Trial Associate

Boston, MA · On-site

$110K - $115K/yr

Ensures receipt, completeness, accuracy, and appropriate filing (Trial Master File, study SharePoint, other study or Olema-specific systems) of clinical and administrative documents * Assists in ...

Clinical Trials Associate

San Carlos, CA · On-site

$40.50 - $55.25/hr

Trial Master File (TMF) * Assist with the management and quality control of electronic Trial Master Files (eTMFs). * Review documents for completeness, accuracy, and TMF filing readiness. * Support ...

Clinical Trials Associate

San Carlos, CA · On-site

$40.50 - $55.25/hr

Trial Master File (TMF) * Assist with the management and quality control of electronic Trial Master Files (eTMFs). * Review documents for completeness, accuracy, and TMF filing readiness. * Support ...

TMF Operations Lead

OR · On-site +1

$33.50 - $45.75/hr

As our Trial Master File expert, you'll partner with Clinical Operations and cross-functional teams to build high-quality TMFs, identify and address risks early, and help ensure our studies are ...

Showing results 21-40

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Infographic showing various Temp Trial Master File Specialist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, and 3% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution.

Contractor

Re-posted 3 days ago


Job description

Company Description

A Few Words About Us - Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Job Summary: 

The primary purpose of this job is to provide support for document approval/finalization and preparation for publishing; submission of documents to clinical study Trial Master File and QC of Trial Master File, including remediation 

Principal Accountabilities:

Assist Medical Writing Operations staff with document approval and notification processes and maintenance of the Trial Master File, including submission of documents and routine QC and remediation. 90% 

Assist Medical Writing staff with document formatting/troubleshooting/reference management. 10% 

Impacts quality of clinical documentation. Liaises with staff across Development Sciences and Global Medical. 

Knowledge & Skills: 

Advanced Microsoft Office skills (Word, PowerPoint, Excel); familiarity with Adobe, Documentum, other systems as needed. 

Strong attention to detail.

Ability to multitask in a fast-paced environment.

Excellent oral and written communication skills. 

Aptitude for learning new systems and technology.

Familiarity with the clinical development process, understanding of trial master file. 

Qualifications

Minimum Education Requirements: Associate's Degree required; Bachelor's Degree preferred.

Minimum Experience Requirements: 1+ year experience in biotech or pharmaceutical company (R&D, Clinical preferred).


Additional Information

With Regards,


Kavita Kumari

Clinical Recruiter

Integrated Resources, Inc

IT REHAB CLINICAL NURSING

Inc. 5000 - 2007-2014 (8th Year)

Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70

Tel: 732-549-2030 x208

Fax: 732-549-5549

Direct: 732-549-5302

www.irionline.com

https://www.linkedin.com/in/rkavita



Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996