Intern CRA - FSO

FTFRA Fortrea France SARL; Paris; On-site; EUR 12,000 - 18,000; Full time

Job summary

Fortrea France SARL is offering a Clinical Research Intern position designed for students or recent graduates. You will support planning, execution, and oversight of clinical trials across multiple departments, gaining exposure to operational, analytical, or data-focused aspects of clinical research.

You will assist with trial documents, site communications, data entry, data management tools, and regulatory submissions, while contributing to literature reviews and audits readiness.

Qualifications

• Enrolled in life sciences/public health/statistics/computer science/pharmacy or related field.
• Interest in clinical research, trial operations, statistical programming, or data management.
• Strong organizational and time-management skills.
• Detail-oriented with a commitment to high-quality work.
• Effective communication and collaboration abilities.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
• Ability to handle confidential information with discretion.

Responsibilities

• Support planning, execution, and oversight of clinical trials across multiple departments.
• Assist in preparation, review, and maintenance of trial documents.
• Support communication with clinical trial sites and data entry processes.
• Contribute to data cleaning, validation, and generation of outputs in statistical programming.
• Assist in development and testing of data management tools and EDC systems.
• Support regulatory submissions materials preparation and compliance tasks.
• Participate in literature reviews and summary of findings relevant to ongoing studies.
• Support internal audits or inspections readiness activities.

Skills

Life sciences background

Organizational skills

Time-management

Communication skills

Microsoft Office Suite

Education

Currently enrolled or recently graduated in life sciences/public health/statistics/computer science/pharmacy or related field

Tools

SAS

R

CTMS

EDC platforms

Job description

Job Overview

The Clinical Research Intern will support one of the following departments - Clinical Operations, Statistical Programming, Data Management, Drug Safety or Project Management, the planning, execution, and oversight of clinical trials. This internship provides hands-on exposure to operational, analytical, or data-focused aspects of clinical research. It is designed for students or recent graduates interested in clinical development, trial management, or data-driven research.

Summary of Responsibilities

• Assisting in the preparation, review, and maintenance of clinical trial documents (e.g., protocols, informed consent forms, case report forms).
• Supporting communication and coordination with clinical trial sites.
• Participating in data entry, tracking, and quality control activities.
• Helping prepare materials for regulatory submissions and ensuring compliance with applicable guidelines.
• Monitoring study progress, including enrollment tracking and visit schedules.
• Supporting statistical programming tasks such as data cleaning, validation, and generation of summary outputs.
• Assisting in the development and testing of data management tools and electronic data capture systems.
• Conducting literature reviews and summarizing findings relevant to ongoing studies.
• Performing administrative tasks to support the assigned team.
• Supporting internal audits or inspections readiness activities.
• Performing other duties as assigned to support the success and efficiency of the department.

Qualifications (Minimum Required)

• Currently enrolled in or recently graduated from a degree program in life sciences, public health, statistics, computer science, pharmacy, or another related field.
• Demonstrated interest in clinical research, trial operations, statistical programming, or data management.
• Strong organizational and time-management skills.
• Detail-oriented with a commitment to high-quality work.
• Effective communication skills and ability to work collaboratively.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
• Ability to handle confidential information with discretion.

Preferred Skills

• Familiarity with Good Clinical Practice (GCP) and clinical trial processes.
• Experience with CTMS, EDC platforms, or statistical software (e.g., SAS, R) is a plus.

Work Environment

Work is performed in an office environment with exposure to electrical office equipment. Occasional drives to site locations with occasional travel both domestic and international.

Physical Requirements

• Frequently stationary for 6-8 hours per day.
• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
• Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
• Regular and consistent attendance.
• Varied hours may be required.

Learn more about our EEO & Accommodations request here.

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