Clinical Research Associate II - France

Fortrea; Paris; À distance; EUR 45 000 - 75 000; Plein temps

Résumé du poste

An established industry player is seeking a Clinical Research Associate II to join their innovative team. This role focuses on ensuring the highest standards in oncology trials, coordinating projects, and protecting patient safety. You will conduct site monitoring, manage project plans, and mentor new staff, playing a vital role in advancing clinical research. With opportunities for professional growth and a comprehensive benefits package, this position offers a chance to make a meaningful impact on global health outcomes. If you're passionate about clinical excellence, this is the perfect opportunity for you.

Prestations

Health and Wellness Programs

Flexible Work Arrangements

Professional Growth Opportunities

Qualifications

• 2+ years of experience in clinical monitoring, especially in oncology.
• Strong understanding of regulatory and drug development processes.

Responsabilités

• Conduct site monitoring and maintain study files for clinical trials.
• Ensure data integrity and compliance with protocols and regulations.

Connaissances

Clinical Monitoring

Regulatory Knowledge

Site Management

Communication Skills

Formation

Bachelor's Degree in Life Sciences

Outils

Clinical Trial Management Systems

Description du poste

Join Fortrea as a Clinical Research Associate II and drive clinical excellence in oncology trials. This role is for upcoming future opportunities that may arise at Fortrea.

As a CRA II, you will ensure clinical studies are conducted to the highest regulatory and quality standards, protecting patient safety and delivering reliable data. You will coordinate designated clinical projects as a Local Project Coordinator and may act as a local client contact as assigned. Your work will help shape the future of clinical research and provide life-changing treatments to patients worldwide.

Summary of Responsibilities :

1. Conduct all aspects of study site monitoring (pre-study initiation, routine, closeout visits) and maintain study files.
2. Manage site-level implementation of project plans and ensure audit readiness.
3. Ensure data integrity and patient protection by verifying adherence to protocols, informed consent, and regulatory requirements.
4. Monitor, review, and resolve data discrepancies and generate accurate trip reports.
5. Act as Lead CRA or Local Project Coordinator overseeing site activities and project progress.
6. Serve as point of contact for clinical trial supplies and vendors.
7. Mentor and assist with the development of new CRA staff as assigned.

Qualifications :

1. At least 2 years of clinical monitoring experience, including oncology therapeutic areas.
2. Strong knowledge of regulatory and drug development processes.
3. Advanced skills in site monitoring, site management, and registry administration.
4. Fluent in the local language and English, with excellent written and verbal communication skills.

Experience :

1. Minimum 1 year of experience in medical, clinical, pharmaceutical, or related fields.
2. Experience in local project coordination or project management.

Benefits :

At Fortrea, we value our team members and offer a comprehensive benefits package, including competitive compensation, health and wellness programs, and opportunities for professional growth. You will also enjoy flexible work arrangements and the chance to make a meaningful impact in cutting-edge clinical research.

Your contribution to Fortrea's success :

In this role, you will help ensure the smooth execution of clinical trials and play a key role in delivering high-quality data and compliance. Your efforts will contribute directly to Fortrea's mission of advancing clinical research and improving global health outcomes. Ready to make an impact? Join us!

Location: Remote

Job ID: LIM1;40

Learn more about our EEO & accommodations request here.

Required Experience :

Key Skills

CSS, Cloud Computing, Health Education, Actuary, Building Electrician

Employment Type : Full-Time

Experience : 1 year

Vacancy : 1