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ERGOMED

Trial Master File Specialist II/Senior TMF, TMF and ALCOA principles experience required

ERGOMED

. Assist with setup and maintenance of the Trial Master File (TMF) .

Posted 11/3/2026full-timeRemote • RomaniaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Trial Master File (TMF) maintenance, quality checks, and adherence to ALCOA+ principles, with strong administrative skills in a clinical research environment. Proficient in Excel and effective in communication, ensuring accurate documentation and reporting.

Highest-signal resume keywords
TMF MaintenanceALCOA PrinciplesExcel ProficiencyQuality Check ExperienceClinical Research Administration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
TMF MaintenanceQuality CheckDocument ProcessingTMF ReconciliationAudit Participation
Soft Skills
Communication SkillsResponsibilityIndependence
Tools & Technologies
Internal Systems
Industry Keywords
Clinical ResearchSOPsCorrective Action PlansPreventative Action PlansProject Management

About the role

Key responsibilities & impact
  • Assist with setup and maintenance of the Trial Master File (TMF)
  • Serve as the main point of contact for TMF-related activities for assigned projects
  • Process and index project documents for the TMF according to project-specific guidelines and relevant SOPs
  • Assist with TMF reconciliation upon study closure
  • Ship files to the client when agreed and prepare the TMF for archiving
  • Track and quality-check documents using internal systems and ALCOA+ principles
  • Prepare study team reports or updates on TMF status as required
  • Support preparations for study-specific audits
  • Attend in-house project audits when required and participate in analysis of audit reports
  • For TMF Specialist II, propose and oversee completion of Corrective and Preventative Action Plans for TMF aspects of the project

Requirements

What you’ll need
  • TMF maintenance and quality check experience
  • Experience with ALCOA Principles
  • Administrative work experience, preferably in an international Clinical Research setting
  • Proficiency in Excel
  • Ability to take responsibility for TMF quality and follow up on topics independently
  • Very good English oral and written communication skills

Benefits

Comp & perks
  • Remote work availability
  • Work-life balance
  • Collaborative, international team environment
  • Career growth opportunities
  • Opportunity to take ownership early
  • Passionate and collaborative team of clinical research, pharmacovigilance, and quality consulting experts