Uploads/files/performs quality control on documents to be submitted to the Trial Master File. Includes identification of missing documentation and follow-up with authors or other stakeholders to ...
Uploads/files/performs quality control on documents to be submitted to the Trial Master File. Includes identification of missing documentation and follow-up with authors or other stakeholders to ...
Oversee CRO management of the Trial Master File (TMF), ensuring completeness and quality. Ensure timely and accurate registration and updates in clinical trial registries (e.g., ClinicalTrials.gov)
New
Oversee CRO management of the Trial Master File (TMF), ensuring completeness and quality. Ensure timely and accurate registration and updates in clinical trial registries (e.g., ClinicalTrials.gov)
New
Senior Clinical Trial Manager
Waltham, MA · On-site
Trial Master File and inspection readiness * Maintain oversight of study TMF completeness and ... Manage vendor deliverables and timelines, escalate risks, and track issue resolution. Required ...
Quick apply
Senior Clinical Trial Manager
Waltham, MA · On-site
Trial Master File and inspection readiness * Maintain oversight of study TMF completeness and ... Manage vendor deliverables and timelines, escalate risks, and track issue resolution. Required ...
Senior Clinical Trial Manager
Waltham, MA · On-site
Trial Master File and inspection readiness * Maintain oversight of study TMF completeness and ... Manage vendor deliverables and timelines, escalate risks, and track issue resolution. Required ...
Senior Clinical Trial Manager
Waltham, MA · On-site
Trial Master File and inspection readiness * Maintain oversight of study TMF completeness and ... Manage vendor deliverables and timelines, escalate risks, and track issue resolution. Required ...
Oversee CRO management of the Trial Master File (TMF), ensuring completeness and quality. Ensure timely and accurate registration and updates in clinical trial registries (e.g., ClinicalTrials.gov)
New
Oversee CRO management of the Trial Master File (TMF), ensuring completeness and quality. Ensure timely and accurate registration and updates in clinical trial registries (e.g., ClinicalTrials.gov)
New
Senior Clinical Trial Manager
Waltham, MA · On-site
Trial Master File and inspection readiness * Maintain oversight of study TMF completeness and ... Manage vendor deliverables and timelines, escalate risks, and track issue resolution. Required ...
Senior Clinical Trial Manager
Waltham, MA · On-site
Trial Master File and inspection readiness * Maintain oversight of study TMF completeness and ... Manage vendor deliverables and timelines, escalate risks, and track issue resolution. Required ...
Clinical Trial Manager
Cambridge, MA · On-site
$140K - $168K/yr
Manage the operational aspects of clinical trials (e.g., study management, site monitoring and management, trial master file (TMF) oversight,) * Coordinate and support regulatory submissions and ...
Quick apply
Clinical Trial Manager
Cambridge, MA · On-site
$140K - $168K/yr
Manage the operational aspects of clinical trials (e.g., study management, site monitoring and management, trial master file (TMF) oversight,) * Coordinate and support regulatory submissions and ...
Clinical Trial Associate
Waltham, MA · On-site
$90K - $124K/yr
Support Trial Master File (TMF) activities, including document filing and quality control checks ... Support sample management activities and basic study logistics * Contribute to the review and ...
Clinical Trial Associate
Waltham, MA · On-site
$90K - $124K/yr
Support Trial Master File (TMF) activities, including document filing and quality control checks ... Support sample management activities and basic study logistics * Contribute to the review and ...
Clinical Trial Associate
$90K - $124K/yr
Support Trial Master File (TMF) activities, including document filing and quality control checks ... Support sample management activities and basic study logistics * Contribute to the review and ...
Clinical Trial Associate
$90K - $124K/yr
Support Trial Master File (TMF) activities, including document filing and quality control checks ... Support sample management activities and basic study logistics * Contribute to the review and ...
Support Trial Master File (TMF) activities, including document filing and quality control checks ... Support sample management activities and basic study logistics * Contribute to the review and ...
Quick apply
Support Trial Master File (TMF) activities, including document filing and quality control checks ... Support sample management activities and basic study logistics * Contribute to the review and ...
Sr. Clinical Trial Associate
Waltham, MA · On-site
$115K - $159K/yr
Support Trial Master File (TMF) management, including document filing and quality control * Assist with development, editing, and distribution of key study documents (e.g., informed consent forms ...
Sr. Clinical Trial Associate
Waltham, MA · On-site
$115K - $159K/yr
Support Trial Master File (TMF) management, including document filing and quality control * Assist with development, editing, and distribution of key study documents (e.g., informed consent forms ...
Sr. Clinical Trial Associate
Waltham, MA · On-site
$115K - $159K/yr
Support Trial Master File (TMF) management, including document filing and quality control * Assist with development, editing, and distribution of key study documents (e.g., informed consent forms ...
Sr. Clinical Trial Associate
Waltham, MA · On-site
$115K - $159K/yr
Support Trial Master File (TMF) management, including document filing and quality control * Assist with development, editing, and distribution of key study documents (e.g., informed consent forms ...
Support Trial Master File (TMF) management, including document filing and quality control * Assist with development, editing, and distribution of key study documents (e.g., informed consent forms ...
Quick apply
Support Trial Master File (TMF) management, including document filing and quality control * Assist with development, editing, and distribution of key study documents (e.g., informed consent forms ...
CTM/ Sr. Clinical Trial Manager
Cambridge, MA · On-site
$164K - $185K/yr
Oversee CRO management of the Trial Master File (TMF), ensuring completeness and quality. Ensure timely and accurate registration and updates in clinical trial registries (e.g., ClinicalTrials.gov)
CTM/ Sr. Clinical Trial Manager
Cambridge, MA · On-site
$164K - $185K/yr
Oversee CRO management of the Trial Master File (TMF), ensuring completeness and quality. Ensure timely and accurate registration and updates in clinical trial registries (e.g., ClinicalTrials.gov)
Clinical Trial Manager
Boston, MA · On-site
Responsible for maintaining internal study documents in the Trial Master File (TMF) and periodically reviewing the CRO TMF for completeness and accuracy. * Support forecasting and management of ...
Clinical Trial Manager
Boston, MA · On-site
Responsible for maintaining internal study documents in the Trial Master File (TMF) and periodically reviewing the CRO TMF for completeness and accuracy. * Support forecasting and management of ...
Senior Clinical Trial Associate
Watertown, MA · On-site
$68K - $94K/yr
Ensure timely maintenance of the Trial Master File (TMF) according to regulatory guidance and ... Manage vendor POs and trial payments (including budget reconciliation), including invoice review ...
Senior Clinical Trial Associate
Watertown, MA · On-site
$68K - $94K/yr
Ensure timely maintenance of the Trial Master File (TMF) according to regulatory guidance and ... Manage vendor POs and trial payments (including budget reconciliation), including invoice review ...
Senior Clinical Trial Manager
Cambridge, MA · On-site
The role will be accountable for clinical trial management, trial master file, site monitoring, study start-up activities, and CRO management. What You Can Expect: * Overall responsibility for the ...
Senior Clinical Trial Manager
Cambridge, MA · On-site
The role will be accountable for clinical trial management, trial master file, site monitoring, study start-up activities, and CRO management. What You Can Expect: * Overall responsibility for the ...
Senior Clinical Trial Associate
Waltham, MA · On-site
$36.25 - $49.25/hr
... manage competing priorities in a dynamic clinical development environment. This role is based in ... Collect, file, reconcile, and track essential documents for the trial master file (TMF); conduct ...
Senior Clinical Trial Associate
Waltham, MA · On-site
$36.25 - $49.25/hr
... manage competing priorities in a dynamic clinical development environment. This role is based in ... Collect, file, reconcile, and track essential documents for the trial master file (TMF); conduct ...
Senior Clinical Trial Associate
Burlington, MA · On-site
$90K - $100K/yr
Manages CRO/Clinical Service Providers (CSPs) interactions, including sponsor oversight of operational functional activities (e.g., study management, monitoring, site management, Trial Master File)
Quick apply
Senior Clinical Trial Associate
Burlington, MA · On-site
$90K - $100K/yr
Manages CRO/Clinical Service Providers (CSPs) interactions, including sponsor oversight of operational functional activities (e.g., study management, monitoring, site management, Trial Master File)
Clinical Trial Associate - Oncology
Bedford, MA · Hybrid
$35.25 - $48/hr
Maintain the Trial Master File (TMF), ensuring completeness, accuracy, and audit readiness ... Excellent planning, coordination, and time management skills * Excellent oral, written, and visual ...
Clinical Trial Associate - Oncology
Bedford, MA · Hybrid
$35.25 - $48/hr
Maintain the Trial Master File (TMF), ensuring completeness, accuracy, and audit readiness ... Excellent planning, coordination, and time management skills * Excellent oral, written, and visual ...
Trial Master File Manager information
See Boston, MA salary details
$48.3K - $55.2K
10% of jobs
$60.4K is the 25th percentile. Wages below this are outliers.
$55.2K - $62.1K
20% of jobs
$62.1K - $68.9K
9% of jobs
$68.9K - $75.8K
10% of jobs
The median wage is $76.8K / yr.
$75.8K - $82.7K
15% of jobs
$82.7K - $89.5K
6% of jobs
$94.9K is the 75th percentile. Wages above this are outliers.
$89.5K - $96.4K
7% of jobs
$96.4K - $103.2K
3% of jobs
$103.2K - $110.1K
14% of jobs
$110.1K - $117K
3% of jobs
$117K - $123.8K
3% of jobs
$48.3K
$82.1K
$123.8K
How much do trial master file manager jobs pay per year?
What are some common challenges faced by trial master file managers, and how can they be addressed?
What is a trial master file manager?
What are the key skills and qualifications needed to thrive as a trial master file manager?
What are the most commonly searched types of Trial Master File jobs in Boston, MA?
The most popular types of Trial Master File jobs in Boston, MA are:
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For Trial Master File Manager jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Trial Master File Manager jobs in Boston, MA look for?
The top searched job categories for Trial Master File Manager jobs in Boston, MA are:
- Clinical Research Manager
- Clinical Research Site Manager
- Sr Clinical Trial Associate
- Associate Clinical Data Manager
- Home Based Clinical Research Associate
- Clinical Trial Recruitment Specialist
- Takeda Pharmaceuticals Clinical Trial Associate
- Remote Clinical Project Manager
- Sr Clinical Data Manager
- Contract Clinical Trial Manager
What cities near Boston, MA are hiring for Trial Master File Manager jobs?
Cities near Boston, MA with the most Trial Master File Manager job openings:

Job 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 Summary:
The primary purpose of this job is to file, QC, and remediate Medical Writing documentation required for Trial Master Files.
Uploads/files/performs quality control on documents to be submitted to the Trial Master File. Includes identification of missing documentation and follow-up with authors or other stakeholders to obtain missing items; performing quality reviews of files and any needed remediation (e.g., follow-up with sources, generating notes to file to explain any discrepancies); and completing file review documentation.
Responsible for ensuring timely filing of TMF documentation; addressing backlog of unfilled documentation; performing periodic review and remediation of TMF.
Qualifications:
Related Document Processing experience with Associate s degree
2+ yrs. with Bachelor's degreeÂ
Quality control experience preferred.
Warm Regards,
Sneha Shrivastava
Clinical Recruiter
Integrated Resources, Inc
IT REHAB CLINICAL NURSING
Tel: (732) 549 2030Â
Fax: (732) 549 5549
Inc. 5000 - 2007, 2008, 2009, 2010, 2011, 2012,2013 & 2014 (8th Year)
Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70
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