eTMF Specialist @Excelya
All Others
Salary unspecified
Remote Location
Employment Type full-time
Posted 3d ago

[Hiring] eTMF Specialist @Excelya

3d ago - Excelya is hiring a remote eTMF Specialist. 💸 Salary: unspecified 📍Location: France

Role Description

The eTMF Specialist plays a key role within the Clinical Development Platform by ensuring the quality, compliance, and inspection readiness of the electronic Trial Master File (eTMF) across global clinical trials. This role requires strong expertise in clinical documentation management, close collaboration with cross‑functional teams, and active involvement in audits and inspections within a regulated environment.

  • Manage the end‑to‑end lifecycle of eTMFs, including setup, maintenance, and close‑out for clinical studies
  • Perform regular quality control checks to ensure document completeness, accuracy, and compliance with regulatory standards
  • Monitor and track TMF metrics and KPIs to ensure inspection readiness
  • Review and approve TMF management plans for internal teams and CROs
  • Act as a Subject Matter Expert (SME), providing guidance and training on eTMF best practices
  • Develop, update, and maintain SOPs, templates, and processes related to TMF management
  • Serve as the main point of contact for eTMF-related queries, audits, and inspections
  • Ensure compliance of the eTMF system with validation and regulatory requirements
  • Manage user access, system updates, and migrations, and assess the impact of new system releases
  • Collaborate with IT teams to resolve system issues and support continuous improvement

Qualifications

  • Bachelor’s or Master’s degree in Health Sciences, Life Sciences, or related field
  • Strong experience in clinical trial documentation management

Requirements

  • Hands‑on experience with Veeva Vault TMF (mandatory)
  • Strong understanding of the DIA TMF Reference Model
  • Experience with TMF metrics, KPIs, and dashboards
  • Strong knowledge of ICH/GCP guidelines and regulatory requirements
  • Understanding of clinical trial documentation lifecycle
  • Knowledge of cross‑functional stakeholders (Clinical, QA, PV, Biometry, etc.)
  • Fluent English (written and spoken)

Benefits

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare. Here’s what makes us unique:

  • We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s leading mid-size CRO with the best employee experience.
  • Our one-stop provider service model—offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects.
  • Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.
  • Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.
Before You Apply
remote Be aware of the location restriction for this remote position: France
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eTMF Specialist @Excelya
All Others
Salary unspecified
Remote Location
Employment Type full-time
Posted 3d ago
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remote Be aware of the location restriction for this remote position: France
Beware of scams! When applying for jobs, you should NEVER have to pay anything. Learn more.
Apply for this position
Did not apply
Applied
Sent Follow-Up
Interview Scheduled
Interview Completed
Offer Accepted
Offer Declined
Application Denied
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