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Trial Master File Manager Jobs in Atlanta, GA (NOW HIRING)

Syneos Health

CRC II (Onsite) - Marietta, GA

Marietta, GA · On-site

$23 - $30.50/hr

Prepare and maintain the Investigator Site File and/ or Trial Master File (TMF) for the study ... Management of daily tasks. * Visit calendar development and maintenance. * Scheduling and attending ...

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 ...

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

Atlanta, GA · On-site

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 · On-site

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

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 ...

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 ...

Morgan & Morgan, P.A.

Trial Attorney

Atlanta, 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 ...

WizeHire, Inc

Criminal Defense Trial Attorney

Atlanta, GA · On-site

$90 - $110/hr

We do hundreds of motions hearings every year and file at least one lengthy memorandum in every ... We use MyCase case management software that has been tweaked for our firm to make our jobs less ...

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Trial Master File Manager information

See Atlanta, GA salary details

$42.8K

$72.7K

$109.6K

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

As of Aug 25, 2026, the average yearly pay for trial master file manager in Atlanta, GA is $72,685.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,400.00 and $89,900.00 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 Atlanta, GA?

The most popular types of Trial Master File jobs in Atlanta, GA are:

What are popular job titles related to Trial Master File Manager jobs in Atlanta, GA?

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

What job categories do people searching Trial Master File Manager jobs in Atlanta, GA look for?

The top searched job categories for Trial Master File Manager jobs in Atlanta, GA are:

Trial Master File Manager jobs near you

Clinical Research Associate (CRA) -Cardiovascular Medical Device

Mirus LLC

Marietta, GA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago

Job description


Role: Clinical Research Associate (CRA) - Cardiovascular Medical Device

Location: Remote

Position Summary:

Assist with the management of cardiovascular clinical studies for MiRus products with a focus on adherence to critical timelines, high-caliber document development and quality data collection. The applicant should possess strong critical thinking skills and the ability to comprehend technical subject matter to effectively contribute to the organization.

Essential Duties and Responsibilities:

  • Contribute to content generation, writing and editing of study protocols, amendments, informed consents, committee charters, study reports, monitoring plans, and other related clinical and regulatory documents.
  • Assist with the management of investigational studies from start through study closure.
  • Engage in new study trial design with cross functional teams, including clinical and pre-clinical research and development groups.
  • Contribute to the development of CRFs
  • Assist with the formulation of instructional materials and training of investigators, study coordinators and associated study site personnel on the conduct of the clinical trials, as applicable.
  • Assist Study Manager with safety monitoring including preparing supporting documentation for CEC and/or DSMB, meetings, agenda, data review, presentations, and updating relevant trackers as applicable.
  • Serve as a point of contact between clinical site investigators and the MiRus team.
  • Work with investigators and site personnel to quickly and effectively resolve discrepancies.
  • May be responsible for patient accruals and tracking payments to sites for clinical study programs
  • Serve as a point of contact between CRO personnel and MiRus.
  • Oversee/support CRO and field study monitors, with monitoring related items and follow-up on study tasks.
  • Monitor ongoing compliance to study protocols in accordance with applicable regulations and GCP, work instructions, guidelines and/or policies.
  • Provide continuous data review of source documents, case report forms, data reports as appropriate.
  • Assist in review of monitoring reports and tracking of action items.
  • Review source documentation to confirm subject eligibility for clinical trials.
  • Track and upload study imaging
  • Manage clinical study documentation (trial master file and study related tracking).
  • Update and design as needed study dashboards, study trackers and other applicable study documents to provide regular updates on trial status to Study Manager
  • Interact with data management, as applicable
  • Support applications and technical files as needed.
  • Assist with preparation for investigators meetings.

Minimum Education and/or Experience:

  • Bachelor’s or Master’s degree in nursing with clinical experience in the cardiac field (CCU, CVOR, Cath Lab) and experience in a clinical research role. CRA certification desired.
  • At least 2 years of experience in clinical research role, with at least 2 years in CRA role, preferably in cardiovascular medical device.
  • Experience in clinical trials and/or post-market registries in the U.S., Australian and/or European Union, with other geographies desired.
  • Current knowledge of medical device clinical trials design and best practices.
  • Proficient knowledge of FDA regulations and ICH/GCP guidelines, guidance documents, and other applicable regulations and standards, and implementation of these standards in the medical device industry, in the U.S. and all countries in which trials are conducted.
  • General application of medical terminology (cardiovascular specific preferred).

Benefits:
MiRus offers competitive compensation, options, full benefits, and relocation assistance.

  • 401(k)
  • Dental insurance
  • Vision insurance
  • Disability insurance
  • Employee assistance program
  • Flexible spending account or Health Savings Account
  • Health insurance
  • Life insurance
  • Paid time off

Schedule:

  • Monday to Friday (8am – 5pm)

Work Location:

  • Remote
  • Position may require domestic travel at least 20-40%