Clinical Research Associate II / Senior Clinical Research Associate (France)

Allucent; Paris; Hybrid; EUR 45,000 - 60,000; Full time

Benefits offered by this job

Competitive salaries and benefits

Departmental study/training

Mentoring opportunities

Internal growth opportunities

Employee referral program

Employee recognition programs

Loyalty Award Program

Job summary

A leading biopharmaceutical company in Paris is seeking a Clinical Research Associate II / Senior Clinical Research Associate to monitor clinical trials and ensure compliance with regulations. The role requires at least 2 years of independent monitoring experience, strong communication skills in English and French, and the ability to manage site relationships. Competitive salary and benefits are offered, with opportunities for professional development.

Qualifications

• Minimum of 2 years as an independent site monitor in clinical trials, ideally in oncology or rare disease.
• Strong understanding of ICH-GCP and regulatory guidelines.
• Comfortable working independently and managing priorities.

Responsibilities

• Independently manage all aspects of monitoring for assigned clinical trials.
• Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
• Build strong site relationships and ensure high-quality data collection.
• Identify and resolve site issues, escalating as needed.
• Mentor and support junior CRAs.

Skills

Leading monitoring activities

Site relationship management

Problem-solving

Clear communication in English and French

Job description

Clinical Research Associate II / Senior Clinical Research Associate (France)

Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA II) or Senior Clinical Research Associate (Sr. CRA) to join our A-team. As a CRA II / Sr. CRA at Allucent, you will independently control and monitor investigational sites, pro‑actively detect issues, and provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice. This position can be either office based (Paris) or remote.

At Allucent™, we are dedicated to helping small‑medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life‑changing therapies to patients in need across the globe.

The role

As a CRA II / Sr. CRA, you will take the lead on monitoring activities, own your sites and relationships with investigators, and be the bridge between sponsor and site. You will mentor junior team members and contribute to our success. Travel throughout France is required.

Main responsibilities

• Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close‑out visits.
• Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
• Build strong site relationships, acting as a primary point of contact and ensuring high‑quality data collection.
• Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.
• Mentor and support junior CRAs, sharing knowledge and best practices.

Requirements

• Experience leading monitoring activities in complex trials, ideally in oncology or rare disease, with a minimum of 2 years as an independent site monitor.
• Strong understanding of ICH‑GCP and regulatory guidelines.
• Clear and confident communicator in English and French.
• Comfortable working independently and managing priorities.
• Willingness to travel in France as required.

Benefits

• Competitive salaries and a comprehensive benefits package.
• Departmental study/training for furthering professional development.
• Mentoring opportunities.
• Internal growth opportunities and career progression.
• Financially rewarding internal employee referral program.
• Eligibility for internal employee recognition programs.
• Eligibility for the Loyalty Award Program.

About Allucent

Our mission is to help bring new therapies to light. At Allucent, you will apply your unique skill set, expertise, and knowledge to build partnerships with our clients as they develop new, life‑improving treatments.

Apply now!

If you are interested in this role, please apply through the button or reach out to Yael Kokernoot.

Disclaimers

Our in‑office work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices. The Allucent Talent Acquisition team manages the recruitment and employment process. Unsolicited resumes sent to Allucent employees will not obligate Allucent to future employment of those individuals.