Clinical Research Associate (France)

Allucent; Paris (TX); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Benefits package

Competitive salary

Training budget

Flexible hours

Buddy program

Career growth

Referral program

Spot bonus

Loyalty awards

Job summary

Allucent is seeking a Clinical Research Associate (CRA) to lead monitoring activities, own site relationships, and bridge sponsor-site communications to ensure trial integrity. The role includes regulatory and startup tasks with travel across France, requiring fluency in English and French and independent work with strong prioritization.

Candidate should have at least 2 years of monitoring experience, knowledge of ICH-GCP, and a flexible, proactive approach to study-startup and site activation

Qualifications

• Experience leading monitoring activities in clinical trials (min 2 years).
• Strong understanding of ICH-GCP and regulatory guidelines.
• Clear and confident communicator in English and French.
• Independent worker with good prioritization.
• Willingness to travel (8 days per month).

Responsibilities

• Independently manage monitoring for trials across phases, including site initiation, routine monitoring, and close-out visits.
• Ensure compliance with protocols, GCP, ICH, SOPs, and regulatory requirements.
• Build strong site relationships as primary contact and ensure high-quality data.
• Identify and resolve site issues, escalating to maintain trial integrity and patient safety.
• Contribute to regulatory affairs, site activation and study-startup activities.

Skills

Monitoring

Site relationships

Travel readiness

Communication

Job description

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.”