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Trial Master File Jobs in Georgia (NOW HIRING)

IQVIA

CRA 1, IQVIA Biotech

Marietta, GA

$71K - $145K/yr

During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the ...

Tucker Ellis LLP

Litigation Paralegal

Atlanta, GA · On-site

Finalize court filings, ensuring accurate citations; verifying compliance with local rules ... Prepare exhibits for motions, hearings, depositions, and trial by labeling, combining, organizing ...

Tucker Ellis LLP

Litigation Paralegal

Atlanta, GA · On-site

Finalize court filings, ensuring accurate citations; verifying compliance with local rules ... Prepare exhibits for motions, hearings, depositions, and trial by labeling, combining, organizing ...

Robert Half

Staff Accountant

Savannah, GA · On-site

$24 - $28/hr

Review master data records and recommend updates that improve the accuracy and consistency of ... Assemble documentation and schedules required for annual filings such as sales tax reports, 1099s ...

Danaher

Principal Clinical Scientist

Atlanta, GA · On-site +1

This role is responsible for clinical trial strategies within the US and EU regions for Danaher ... Author and review clinical and regulatory documentation-including study reports, technical files ...

Department of Justice

Paralegal Specialist

Macon, GA · On-site

$61K/yr

OR a Master's or equivalent graduate degree or higher; OR 2 full years of progressively higher ... files to identify relevant issues and potential evidence; conducting legal research concerning ...

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How much do trial master file jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for trial master file in Georgia is $30.90, according to ZipRecruiter salary data. Most workers in this role earn between $20.01 and $37.59 per hour, depending on experience, location, and employer.

What is a trial master file?

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 typical responsibilities and daily tasks of a trial master file 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 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 most commonly searched types of Trial Master File jobs in Georgia?

The most popular types of Trial Master File jobs in Georgia are:

What are popular job titles related to Trial Master File jobs in Georgia?

For Trial Master File jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Trial Master File jobs in Georgia look for?

The top searched job categories for Trial Master File jobs in Georgia are:

What cities in Georgia are hiring for Trial Master File jobs?

Cities in Georgia with the most Trial Master File job openings:

Trial Master File jobs near you
Infographic showing various Trial Master File job openings in Georgia as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 81% Full Time, 13% Part Time, and 4% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $64,280 per year, or $30.9 per hour.

Clinical Data Manager II

Katalyst HealthCares & Life Sciences

Atlanta, GA

Full-time

Re-posted 23 days ago

Job description

Clinical Data Management Specialist

Responsibilities:

Maintain and update EDC user access across multiple clinical studies

Track and manage user access requests in coordination with CRAs and EDC vendors

Curate and maintain standardized tracking spreadsheets for both internal and external use

Transfer verified data from working trackers to production master user lists

Respond to and resolve user-related queries from study teams and EDC builders

Prepare and upload CDM documents to the Trial Master File (TMF) in compliance with internal SOPs and TMF standards

Track document status and ensure completeness and accuracy of TMF content

Collaborate with Sr. CDMs to ensure documents are audit-ready and filed in a timely manner

Assist with study startup, maintenance, and closeout CDM activities as needed

Participate in team meetings, training sessions, and cross-functional collaboration

Support documentation and version control for CDM tools and templates

Maintain clear and organized records of work performed

All other duties as assigned

Requirements:

Bachelor's degree from an accredited institution with a major in Life Sciences, Computer Science, or relevant field of study; or equivalent practical experience.

6+ years of Clinical Data Management experience in biotechnology or pharmaceutical industry with excellent understanding of late phase clinical drug development processes required

Ability to perform well-defined procedures initially with supervision, and after direction is provided, work independently

Ability to work effectively in a team-oriented environment

Flexibility to adapt to changing project requirements and timelines

Excellent attention to detail and organizational skills

Strong communication and collaboration abilities

Proficiency in Microsoft Excel, Word, and document management tools

Strong organizational skills to manage multiple tasks and projects simultaneously

Preferred:

Experience with EDC systems (e.g., Medidata Rave, Oracle InForm)

Familiarity with TMF structure and regulatory filing practices

Understanding of GCP, GCDMP, and clinical trial workflows

Katalyst Healthcares & Life Sciences logo

About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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