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Remote Trial Master File Jobs in Raleigh, NC (NOW HIRING)

IQVIA

Trial Delivery Manager, Multi TA

Durham, NC · Remote

Clinical Trial Management & Central Trial Oversight (FSP Model) Home Based Remote Role - East Coast ... Oversee trial documentation, filing, archiving, and retention. * Create, review, and maintain trial ...

RTI International

Senior Biostatistician

Raleigh, NC · On-site +1

Implement target trial emulation analyses using real-world data sources. * Develop simple to ... Master's degree and 6 years of experience, PhD and 1 years of experience, or equivalent combination ...

RTI International

Senior Biostatistician

Raleigh, NC · On-site +1

Implement target trial emulation analyses using real-world data sources. * Develop simple to ... Master's degree and 6 years of experience, PhD and 1 years of experience, or equivalent combination ...

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All JobsTrial Master File JobsRemote Trial Master File JobsRemote Trial Master File Jobs in Raleigh, NC

Remote Trial Master File information

See Raleigh, NC salary details

$11

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$22

How much do remote trial master file jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for remote trial master file in Raleigh, NC is $17.24, according to ZipRecruiter salary data. Most workers in this role earn between $15.43 and $18.46 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Remote Trial Master File (TMF) Specialist, and why are they important?

To thrive as a Remote Trial Master File (TMF) Specialist, you need a solid understanding of clinical trial processes, regulatory requirements (such as ICH-GCP), and experience with TMF management, often supported by a degree in life sciences or a related field. Familiarity with electronic TMF (eTMF) systems, document management software, and compliance tracking tools is typically required. Attention to detail, organizational skills, and strong communication are vital soft skills to ensure accurate documentation and effective collaboration across remote teams. These skills and qualifications are crucial for maintaining regulatory compliance, ensuring data integrity, and supporting the smooth conduct of clinical trials.

What is the difference between Remote Trial Master File vs Clinical Trial Associate?

AspectRemote Trial Master FileClinical Trial Associate
CredentialsTypically requires knowledge of GCP, ICH guidelines, and document managementRequires knowledge of clinical trial processes, GCP, and data entry
Work EnvironmentRemote, document management systems, cloud-based platformsOffice or site-based, assisting with trial coordination and data collection
Industry UsageUsed across pharmaceutical, biotech, and CROs for document oversightCommonly employed in clinical research teams for trial support

The Remote Trial Master File focuses on managing and maintaining essential trial documents remotely, ensuring compliance and accessibility. In contrast, a Clinical Trial Associate supports trial activities on-site or remotely, handling data collection and coordination. Both roles are vital in clinical research but differ mainly in scope and responsibilities.

What are the main challenges of managing a Trial Master File (TMF) remotely, and how can they be addressed?

Managing a TMF remotely often presents challenges such as maintaining document version control, ensuring regulatory compliance, and facilitating timely collaboration across dispersed teams. To address these, many organizations utilize secure cloud-based eTMF systems that allow real-time access and updates, implement clear document management protocols, and schedule regular virtual check-ins with team members. Strong communication skills and familiarity with electronic documentation tools are essential for success in this remote environment.

What is a Remote Trial Master File (TMF) and what does the role involve?

A Remote Trial Master File (TMF) professional is responsible for managing and maintaining essential documents related to clinical trials in a digital or remote environment. This role ensures that all regulatory and compliance requirements are met by organizing, tracking, and archiving important trial documentation. Working remotely, TMF specialists collaborate with clinical research teams, auditors, and regulatory authorities to ensure data integrity and readiness for inspections. The job often involves using specialized electronic TMF (eTMF) systems to facilitate secure access and management of files from different locations.
What are the most commonly searched types of Trial Master File jobs in Raleigh, NC? The most popular types of Trial Master File jobs in Raleigh, NC are:
What are popular job titles related to Remote Trial Master File jobs in Raleigh, NC? For Remote Trial Master File jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Remote Trial Master File jobs in Raleigh, NC look for? The top searched job categories for Remote Trial Master File jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Remote Trial Master File jobs? Cities near Raleigh, NC with the most Remote Trial Master File job openings:
Remote Trial Master File jobs near you
Clinical Trials Associate - US - Remote

Clinical Trials Associate - US - Remote

Worldwide Clinical Trials

Durham, NC • On-site, Remote

$16.83 - $33.65/hr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Who we are

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

What the Clinical Trial Associate does at Worldwide

As a Clinical Trials Associate, you are responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.

What you will do

  • Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)

  • Maintain and quality audit to assure the most recent revisions of documents are on project portals

  • Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File

  • Maintain version and quality control of project documentation and submit to trial master file

  • Assist with the tracking and maintenance of project related information, including site medical question and answer log

What you will bring to the role

  • Excellent written and verbal English as well as fluency of the language of the country of location

  • Ability to handle multiple tasks and exercise independent judgment

  • Strong attention to detail and focus on quality of work

  • Strong organizational and problem-solving skills

  • Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint

Your experience

  • Degree level qualification or equivalent experience plus a minimum of one years' experience in a related role

  • Skill sets and proven performance equivalent to the above

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):


United States of America - $16.83 - $33.65


The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

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