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Trial Master File Jobs in Delaware (NOW HIRING)

Ensure the timely submission of documents to regulatory authorities and maintain the trial master file (eTMF). Qualifications * Minimum 3 years of experience in Clinical Study Start-Up (full-time)

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 ...

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 ...

CRA 2, Oncology, IQVIA

Wilmington, DE · On-site

$87.20K - $145.30K/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 ...

... Trial Master File. - Contribute to the production of study start-up documents, ensuring template and version compliance. - Create and/or import clinical-regulatory documents into the A New Global ...

... Trial Master File. - Contribute to the production of study start-up documents, ensuring template and version compliance. - Create and/or import clinical-regulatory documents into the A New Global ...

... Trial Master File. - Contribute to the production of study start-up documents, ensuring template and version compliance. - Create and/or import clinical-regulatory documents into the A New Global ...

... Trial Master File. - Contribute to the production of study start-up documents, ensuring template and version compliance. - Create and/or import clinical-regulatory documents into the A New Global ...

Take operational responsibility for correct setup and ongoing maintenance of the local electronic Trial Master File (eTMF) and Investigator Study File (ISF), ensuring document tracking in accordance ...

Study Contracts Manager

Wilmington, DE · Hybrid

$86.40K - $115.50K/yr

Ensure that all study documents are ready for final archiving and sign-off completion of the local part of the Trial Master File. Contribute to process improvements, knowledge transfer and best ...

Study Contracts Manager

Wilmington, DE · Hybrid

$86.40K - $115.50K/yr

Ensure that all study documents are ready for final archiving and sign-off completion of the local part of the Trial Master File. Contribute to process improvements, knowledge transfer and best ...

Study Contracts Manager

Wilmington, DE · On-site

$86.40K - $115.50K/yr

... part of the Trial Master File. • Contribute to process improvements, knowledge transfer and best practice sharing Essential Skills/Experience: - Bachelor's degree in relevant discipline • ...

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Trial Master File information

See Delaware salary details

$10

$37

$72

How much do trial master file jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for trial master file in Delaware is $37.30, according to ZipRecruiter salary data. Most workers in this role earn between $24.16 and $45.38 per hour, depending on experience, location, and employer.

What is a Trial Master File job?

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 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 typical responsibilities and daily tasks of a Trial Master File (TMF) 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 most commonly searched types of Trial Master File jobs in Delaware? The most popular types of Trial Master File jobs in Delaware are:
What are popular job titles related to Trial Master File jobs in Delaware? For Trial Master File jobs in Delaware, the most frequently searched job titles are:
Infographic showing various Trial Master File job openings in Delaware as of May 2026, with employment types broken down into 1% Internship, 36% Full Time, 58% Part Time, 2% Temporary, 2% Contract, and 1% Nights. Highlights an 81% Physical, 5% Hybrid, and 14% Remote job distribution, with an average salary of $77,591 per year, or $37.3 per hour.
Director, Global Trial Master File

Director, Global Trial Master File

Incyte Corporation

Wilmington, DE • On-site

$32.50 - $44.50/hr

Full-time

Posted 11 days ago


Job description

Overview
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
Job Summary (Primary function)
This role provides enterprise leadership for Trial Master File (TMF) strategy, governance, and execution across a global clinical portfolio and is accountable for end-to-end TMF operations, including oversight of internal teams, FSPs, CRO partners, and enabling technologies. The role ensures inspection readiness, regulatory compliance, and scalable operations while driving continuous improvement and modernization of TMF practices.
Essential Functions of the Job (Key responsibilities)
Strategic Leadership & Governance:
• Define and lead the global TMF strategy, governance framework, and operating model
• Establish inspection-readiness standards aligned with ICH-GCP and global regulations
• Serve as escalation point for TMF risks, compliance issues, and inspection outcomes
People Leadership:
• Lead and develop a global team of TMF professionals across regions and partners
• Drive workforce planning, capability building, and performance management
• Foster an inclusive culture of accountability, quality, and continuous improvement
Operational Oversight:
• Ensure consistent TMF execution across studies, CROs, and regions
• Own KPIs, quality metrics, and timeliness of TMF deliverables
• Oversee TMF consolidation, archival, and retention strategies
Inspection & Audit:
• Lead TMF support for regulatory inspections and internal audits
• Review findings, approve CAPAs, and ensure sustainable remediation
Process & Innovation:
• Own global TMF SOPs, work instructions, and TMF Index Model
• Drive system optimization (e.g., Veeva Vault) and digital innovation
• Leverage automation and data insights to improve TMF quality and efficiency
Qualifications (Minimal acceptable level of education, work experience, and competency)
• Degree (such as Bachelor's) or equivalent experienced required; advanced degree or equivalent experience preferred
• Significant experience in TMF or clinical document management (typically 8-10+ years, or equivalent experience)
• Experience managing global teams and vendors
• Strong knowledge of ICH-GCP and regulatory requirements
• Experience with eTMF systems (such as Veeva Vault, or similar systems)
• Familiarity with CDISC TMF Reference Model
• Strong leadership, communication, and problem-solving skills
• Experience in global, matrixed organizations
• Willingness to travel up to 20%, both domestic and international. Reasonable accommodations will be provided to support candidates with disabilities.
Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
We Respect Your Privacy
Learn more at: http://www.incyte.com/privacy-policy
The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.
You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.
You can learn more about Incyte's data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte's data protection officer, and your supervisory authority (if applicable).
Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.
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