eTMF Specialist – Global Trials, Hybrid/Remote (2 days)

Pierre Fabre Pharmaceuticals Inc.; Toulouse; Hybrid; EUR 50,000 - 70,000; Full time

Benefits offered by this job

Incentives

Profit-sharing

Health insurance

25 days personal holidays

Public transport participation

Job summary

Pierre Fabre Pharmaceuticals Inc. is seeking an eTMF Specialist for a full-time position in Toulouse. The specialist will oversee the eTMF system to ensure compliance, manage documentation, and support audits for global clinical trials.

The ideal candidate has at least 5 years of experience in clinical trial documentation management and a strong knowledge of ICH/GCP guidelines. This role offers an attractive remuneration package and up to 2 days of teleworking after the trial period.

Qualifications

• Minimum 5 years of experience in clinical trial documentation management.
• 3 years in an eTMF-focused role, ideally.
• Hands-on experience with Veeva environments.

Responsibilities

• Oversee the electronic Trial Master File (eTMF) system.
• Perform regular quality control checks.
• Ensure compliance with validation requirements.

Skills

Clinical trial documentation management

eTMF management

Veeva Vault

ICH/GCP guidelines

Project management

Education

Bachelor’s or master’s degree in health sciences or related field

Tools

TMF Veeva Vault

Job description

Pierre Fabre Pharmaceuticals Inc. is seeking an eTMF Specialist for a full-time position in Toulouse. The specialist will oversee the eTMF system to ensure compliance, manage documentation, and support audits for global clinical trials.

The ideal candidate has at least 5 years of experience in clinical trial documentation management and a strong knowledge of ICH/GCP guidelines. This role offers an attractive remuneration package and up to 2 days of teleworking after the trial period.