Clinical Research Associate - Oncology

Excelya Group; Paris; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading clinical research organization in France is seeking a Clinical Research Associate specializing in oncology. You will contribute to critical cancer clinical trials, overseeing monitoring and compliance throughout the study lifecycle. The ideal candidate has at least 2 years of experience in oncology trials, possesses strong communication and organizational skills, and is fluent in both English and French. This position offers a collaborative environment focused on scientific excellence and patient care.

Qualifications

• Minimum of 2 years experience as a Clinical Research Associate with a focus on oncology.
• Proficient understanding of ICH-GCP guidelines.
• Fluent in English and French, effective communication in both.

Responsabilités

• Conduct site monitoring and close-out visits for oncology clinical trials.
• Ensure compliance with protocols and regulatory requirements.
• Maintain communication with investigators and site staff.

Connaissances

Clinical trial methodologies

Regulatory requirements

Communication skills

Organizational skills

Problem-solving skills

Formation

Bachelor’s degree in Life Sciences

Nursing

Pharmacy

Description du poste

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations, particularly in the field of Oncology. As a Clinical Research Associate specializing in this area, you will play a crucial role in ensuring the successful conduct of oncology clinical trials, while supporting innovative cancer therapies that make a real difference in patients’ lives.

Main Responsibilities

• Conduct site monitoring, and close-out visits for oncology clinical trials.
• Ensure compliance with protocols, ICH‑GCP guidelines, and regulatory requirements throughout the study lifecycle.
• Maintain effective communication with investigators and site staff, providing ongoing support and guidance.
• Review study‑related documentation and assist in the resolution of any issues related to data collection and study procedures.
• Prepare for and participate in audits and inspections, ensuring the sites are inspection‑ready at all times.
• Track and report any deviations, adverse events, and other issues to the relevant stakeholders.
• Assist in the development and updates of study protocols and informed consent forms specifically for oncology studies.

About You

• Experience: Minimum of 2 years experience as a Clinical Research Associate, with a strong background in oncology clinical trials.
• Skills: Proficient understanding of clinical trial methodologies and regulatory requirements. Excellent communication, organizational, and problem‑solving skills.
• Education: Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Languages: Fluent in English and French, with the ability to communicate effectively in both languages.

Why Join Us?

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.