Remote TMF Compliance & Documentation Specialist

Alimentiv

London

On-site

CAD 55,000 - 75,000

Full time

14 days+
Application generator

An application made for this job — a tailored resume and cover letter that speak straight to the posting.

Get past ATS filters

Benefits offered by this job

Bonus

Job summary

Alimentiv is seeking a detail-oriented TMF Coordinator to join our TMF Operations team. You will maintain quality, completeness, and compliance of TMF documentation aligned with global regulatory requirements, ensuring inspection readiness and supporting clinical trial execution.

Responsibilities include filing and indexing TMF documents in eTMF systems, performing QC checks, and collaborating with cross-functional study teams.

Qualifications

  • Bachelor’s degree in Life Sciences or related field (preferred).
  • 1–3 years experience in clinical trials TMF management.
  • Working knowledge of eTMF platforms and regulatory requirements.
  • Strong understanding of clinical trial record management and quality standards.
  • Remote work capability.

Responsibilities

  • Maintain TMF structures (paper and electronic) and ensure compliance with ICH-GCP, FDA, and EMA regulations.
  • File, classify, and index TMF documents with version control and naming conventions.
  • Perform TMF QC checks and address missing or inconsistent records.
  • Support inspection readiness, audits, and health checks with accurate reporting.
  • Collaborate with study teams and stakeholders to manage documentation and timelines.

Skills

Attention to detail
Organization
Communication
Stakeholder engagement
Analytical thinking

Education

Bachelor’s degree in Life Sciences or related field

Tools

Veeva Vault
Phlexglobal
Trial Interactive
Excel
SharePoint

Job description

Alimentiv is seeking a detail-oriented TMF Coordinator to join our TMF Operations team. You will maintain quality, completeness, and compliance of TMF documentation aligned with global regulatory requirements, ensuring inspection readiness and supporting clinical trial execution.

Responsibilities include filing and indexing TMF documents in eTMF systems, performing QC checks, and collaborating with cross-functional study teams.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Remote TMF Coordinator: Compliance & Document Control
Remote TMF Coordinator: Compliance & Document Control

Alimentiv • Montreal (administrative region)

On-site
CAD 42,000 - 70,000
Bonus
Remote TMF Coordinator: Compliance & Documentation
Remote TMF Coordinator: Compliance & Documentation

Alimentiv • Vancouver

On-site
CAD 42,000 - 70,000
Bonus
Remote work
TMF Associate
TMF Associate

Alimentiv • Montreal

On-site
CAD 52,500 - 87,500
TMF Compliance Associate – Remote
TMF Compliance Associate – Remote

Alimentiv • Montreal

Hybrid
CAD 52,500 - 87,500
Trial Master Files Representative
Trial Master Files Representative

Triwill Group • Canada

On-site
CAD 45,000 - 65,000
Coordinateur TMF II - Travail à domicile
Coordinateur TMF II - Travail à domicile

Indero (formerly Innovaderm) • Montreal (administrative region)

On-site
CAD 55,000 - 75,000
Flexible work schedule
Permanent full-time position
Comprehensive benefits package
+2
Remote Trial Master File Coordinator
Remote Trial Master File Coordinator

Triwill Group • Canada

Hybrid
CAD 45,000 - 65,000
Lead Medical Writer — Regulatory & Publications
Lead Medical Writer — Regulatory & Publications

Alimentiv • Ottawa

On-site
CAD 90,000 - 130,000
French-Speaking Clinical Trials Specialist - Hybrid/Remote
French-Speaking Clinical Trials Specialist - Hybrid/Remote

Emerald Clinical • Quebec

Hybrid
CAD 60,000 - 90,000
Competitive salary
Hybrid/Remote work
Career growth
+2
M&A Associate
M&A Associate

mason group • Toronto

On-site
CAD 103,000 - 129,000