Clinical Research Associate (France)

Allucent; Paris; Hybride; EUR 55 000 - 85 000; Plein temps

Avantages offerts par ce poste

Flexible working hours

Training budget

Study/Training budget for professional

Career progression

Résumé du poste

Allucent is seeking a Clinical Research Associate (CRA) to lead site monitoring and manage relationships with investigators across France. You will own monitoring activities from site initiation through close-out, ensuring trial integrity and patient safety while collaborating with a multidisciplinary team.

You will work in a hybrid model with some in-office requirements, traveling as needed to study sites.

Qualifications

• Experience leading monitoring activities in complex trials.
• Strong understanding of ICH-GCP and regulatory guidelines.
• Fluent in English and French with clear communication.
• Ability to work independently and manage competing priorities.
• Willingness to travel, approx. 8 days per month.

Responsabilités

• Independently manage all monitoring activities for assigned trials across study phases.
• Ensure compliance with protocols, ICH-GCP, SOPs, and regulatory requirements.
• Build strong site relationships as primary contact and ensure high-quality data collection.
• Identify and resolve site issues to maintain trial integrity and patient safety.
• Support regulatory affairs, site activation and study-startup activities.

Connaissances

Monitoring leadership

ICH-GCP

English

French

Independent work

Travel readiness

Description du poste

About Allucent™

At Allucent™, our mission is to shine a light on new therapies that improve lives. When you join our team, you’ll use your unique skills, expertise, and knowledge to forge meaningful partnerships with clients while helping them turn groundbreaking ideas into life-changing treatments.

If you’re passionate about advancing pharmaceuticals and biologics, fueled by an entrepreneurial spirit, and eager to collaborate with top minds across science, business, and operations, we’d love to connect. Together we can accelerate innovation and grow side by side, making a last impact on patients worldwide.

Together we SHINE. Find more information about our values.

The role

Bring your monitoring expertise to the forefront of innovation.We are looking for a Clinical Research Associate (CRA)to join our A-team. As aCRA, you will take the lead on monitoring activities, owning your sites and relationships with investigators. You’ll be the bridge between sponsor and site, ensuring trial integrity while being supported by a collaborative, experienced team. This includes work related to regulatory affairs, site activation processes—including contracting and start-up activities to ensure smooth and compliant study execution. You will travel throughout France.

Main responsibilities:

• Independently manage all aspectsof monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
• Ensure compliancewith 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.
• Activities aroundregulatory affairs, site activationandstudy-startup.

To be successful you will possess:

You’re an experienced CRA ready to take the next step with a company that truly values your expertise and independence. You thrive in an agile, collaborative environment and want to be part of a team making a real impact.

• Experience in leading monitoring activities in complex trials with a minimum of 2 years’ experience.
• Strong understanding ofICH-GCPandregulatory guidelines.
• Clear and confident communicator inEnglish and French.
• Comfortable working independently and managing priorities.
• Willingness to travel, as required (8 DOS per month).

Benefits of working at Allucent include:

• Comprehensive benefits package per location
• Competitive salaries per location
• Departmental Study/Training Budget for furthering professional development
• Flexible Working hours (within reason)
• Participation in our enriching Buddy Program as a new or existing employee
• Internal growth opportunities and career progression
• Financially rewarding internal employee referral program
• Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
• Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees

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 for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third‑party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third‑party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”