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

Alimentiv

Consulting Statistician

Raleigh, NC · On-site +1

$110K - $184K/yr

... remote based, Canada or USA) Statistical Consulting Services * Communicates with clients and ... Candidates should posses a Master's degree and a minimum of 4-6 years of related experience.

Alimentiv

Consulting Statistician

Raleigh, NC · Remote

... remote based, Canada or USA) Statistical Consulting Services * Communicates with clients and ... Candidates should posses a Master's degree and a minimum of 4-6 years of related experience.

Aprio

Senior Director, Resource Management

Raleigh, NC · On-site +1

$225K - $300K/yr

Master's degree preferred. * CPA certification or experience within a CPA-led professional services ... remote and hybrid options What's in it for you: - Working with an industry leader : Be part of a ...

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Remote Trial Master File information

See Raleigh, NC salary details

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

As of Jun 20, 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

Consulting Statistician

Alimentiv

Raleigh, NC • On-site, Remote

$110K - $184K/yr

Full-time

Posted 29 days ago

Job description

As a member of Alimentiv's Statistical Center of Excellence, the Consulting Statistician is responsible for the research, development, and application of innovative biostatistical methods to support clients in clinical study design and implementation. This role advises internal and external clients on statistical planning, study design, data analyses, reporting and interpretation in accordance with project, regulatory and Alimentiv quality standards. Maintains contemporaneous knowledge of statistical methods, industry standards, and regulatory requirements in assigned therapy areas. Provides statistical education and communicates abstract statistical concepts in a manner such that non-statistical colleagues and clients can make informed decisions. Demonstrates thought leadership though contributions to website content and scientific publications and by delivering presentations at conferences or via webinar. Contributes to business development opportunities by meeting with potential clients and contributing to study proposals and capabilities presentations
 
Positions available: 1 (remote based, Canada or USA)
Statistical Consulting Services
  • Communicates with clients and internal stakeholders to understand their statistical and clinical needs. Provides recommendations, guidance, and education on statistical concepts. Creates supplementary materials such as slides or reports to assist in communication and understanding of recommendations and concepts.  Provides critique of and recommendations for study design after investigating innovative methods, accepted industry standards, and regulatory requirements.
  • Prepares statistical analysis plans and oversee project data collection, management, and analysis, with input from the project team, incorporating details regarding the type of information collected, sample size, randomization procedures, table and listing shells, project statistical policies, protocols, and methodology to be used to appropriately translate scientific questions into statistical hypotheses.
  • Reviews, edits, and assists in preparing statistical sections of study synopses, protocols, reports, publications, or presentations in collaboration with clients and internal stakeholders ensuring statistical analyses adhere to trial, sponsor, organizational and regulatory requirements, and best practices.
  • Advises and consults with various departments internally ensuring that strategies include critical project success factors.
  • Oversees and supports project teams in relevant studies; analyzes implementation gaps and works with relevant stakeholders to close them.
Professional Development and Thought Leadership
  • Stays up to date on new innovations in statistical methods, especially in study design relating to chosen or assigned areas of focus.
  • Reviews statistical research papers, learning new statistical techniques and methodologies, and maintaining subject matter expertise.
  • Reviews literature related to clinical research, assigned therapy areas and in the areas of clients' studies to pair with statistical knowledge to provide guidance that is innovative and in line with the needs and standards.
  • Represents Alimentiv at relevant scientific meetings and congresses and attends trainings relating to statistics, clinical research, and medical areas of interest to continue knowledge growth and expertise.
Business Development Support
  • Working in conjunction with the Statistics and Medical Research and Development teams, develops and presents new and novel clinical trial designs and processes and statistical methodologies into publishable and promotable scientific operations and results.
  • Creates materials such as white papers, case studies, and statistical education materials for presentation and posting on Alimentiv websites to foster client relationship development and attract new clients.
  • Leads or supports strategy discussions and development of proposals for Statistical Center of Excellence projects.
  • Provides the proposal lead and functional leads with information necessary to prepare an accurate proposal that meets the strategy parameters. 
  • Involved in frequent client meetings/presentations and responsible for transferring knowledge to applicable project team members regarding the proposal/study strategy at the time of a bid defense.
Qualifications
  • Candidates should posses a Master's degree and a minimum of 4-6 years of related experience. Advanced degrees in Statistics/Biostats is considered an asset.
  • The ability to communicate abstract concepts
  • Highly refined oral and written communication skills
  • High level of presentation skills
$110,500 - $184,000 a year
Stay Alert to Recruitment Scams
We have been made aware of individuals posing as our recruiters and contacting candidates with fraudulent opportunities. Our hiring process always includes direct engagement with a recruiter or hiring manager, and we will never ask for sensitive personal information early in the process. Official communication will only come from our company email domains. If something doesn't feel right, we encourage you to verify before responding.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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