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Trial Master File Manager Jobs in Georgia (NOW HIRING)

IQVIA

CRA 1, IQVIA Biotech

Marietta, GA · On-site

$71K - $145K/yr

... site management activities. In this position, you will ensure that assigned study sites conduct ... the Trial Master File (TMF) and the Investigator Site File (ISF). A central part of this role ...

Morgan & Morgan, P.A.

Trial Attorney

Marietta, GA

Our attorneys are privy to world-class case docket management software, litigation resources, and a ... Drafting and filing of litigation documents to include pleadings, discovery requests, discovery ...

Morgan & Morgan, P.A.

Trial Attorney

Augusta, GA

Our attorneys are privy to world-class case docket management software, litigation resources, and a ... Drafting and filing of litigation documents to include pleadings, discovery requests, discovery ...

Morgan & Morgan, P.A.

Trial Attorney

Atlanta, GA

Our attorneys are privy to world-class case docket management software, litigation resources, and a ... Drafting and filing of litigation documents to include pleadings, discovery requests, discovery ...

Morgan & Morgan, P.A.

Trial Attorney

Alpharetta, GA

Our attorneys are privy to world-class case docket management software, litigation resources, and a ... Drafting and filing of litigation documents to include pleadings, discovery requests, discovery ...

Morgan & Morgan, P.A.

Trial Attorney

Alpharetta, GA

Our attorneys are privy to world-class case docket management software, litigation resources, and a ... Drafting and filing of litigation documents to include pleadings, discovery requests, discovery ...

Morgan & Morgan, P.A.

Trial Attorney

Marietta, GA · On-site

Drafting and filing of litigation documents to include pleadings, discovery requests, discovery ... Ability to manage high volume of litigation cases * Excellent client service and communication ...

Morgan & Morgan, P.A.

Trial Attorney

Augusta, GA · On-site

Drafting and filing of litigation documents to include pleadings, discovery requests, discovery ... Ability to manage high volume of litigation cases * Excellent client service and communication ...

Morgan & Morgan, P.A.

Trial Attorney

Alpharetta, GA · On-site

Drafting and filing of litigation documents to include pleadings, discovery requests, discovery ... Ability to manage high volume of litigation cases * Excellent client service and communication ...

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All JobsTrial Master File JobsTrial Master File Manager JobsTrial Master File Manager Jobs in Georgia

Trial Master File Manager information

See Georgia salary details

$37.6K

$63.8K

$96.3K

How much do trial master file manager jobs pay per year?

As of Sep 3, 2026, the average yearly pay for trial master file manager in Georgia is $63,821.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,900.00 and $78,900.00 per year, depending on experience, location, and employer.

What is a trial master file manager?

A Trial Master File Manager is a professional responsible for overseeing the creation, maintenance, and quality control of the Trial Master File (TMF) in clinical research. The TMF is a collection of essential documents that allow the conduct of a clinical trial to be reconstructed and evaluated. The manager ensures that all documents are complete, accurate, and compliant with regulatory requirements throughout the trial's lifecycle. They work closely with clinical teams, auditors, and regulatory authorities to guarantee readiness for inspections and audits. Their role is crucial for maintaining transparency and credibility in clinical research processes.

What are the key skills and qualifications needed to thrive as a trial master file manager?

To thrive as a Trial Master File Manager, you typically need a strong background in clinical research, regulatory requirements, and document management, often supported by a degree in life sciences or a related field. Familiarity with electronic Trial Master File (eTMF) systems, GCP guidelines, and relevant industry certifications like DIA's TMF Professional Certification is important. Attention to detail, organizational skills, and effective communication help ensure TMF integrity and coordination across cross-functional teams. These skills are crucial for maintaining regulatory compliance, audit readiness, and efficient clinical trial operations.

What are some common challenges faced by trial master file managers, and how can they be addressed?

Trial Master File Managers often encounter challenges such as ensuring TMF completeness, maintaining regulatory compliance, and coordinating document submissions across multiple stakeholders. Keeping documents up-to-date and audit-ready requires strong attention to detail and effective communication with clinical teams, vendors, and sponsors. Leveraging electronic TMF systems, implementing standardized processes, and promoting regular training can help address these challenges and ensure the integrity of the TMF throughout a study.

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 Manager jobs in Georgia?

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

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

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

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

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

Trial Master File Manager jobs near you
Infographic showing various Trial Master File Manager job openings in Georgia as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $63,821 per year, or $30.7 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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