Sr Clinical Research Associate Contractor (France)

Allucent; Paris; On-site; EUR 65,000 - 90,000; Full time

Job summary

Allucent is seeking a Contractor Clinical Research Associate to lead monitoring activities for pivotal trials, ensuring adherence to protocol and GCP while managing site relationships across study phases. The role emphasizes independence, proactive issue resolution, and collaboration with a global team.

You will travel as required, with hybrid work expectations and a focus on quality data and patient safety in line with regulatory standards.

Qualifications

• At least 5 years leading monitoring activities in complex oncology or rare disease trials.
• Strong knowledge of ICH-GCP and regulatory guidelines.
• Fluent in English; Hebrew language proficiency is required.

Responsibilities

• Independently manage site monitoring for assigned trials across study phases.
• Ensure protocol, GCP, ICH, SOP, and regulatory compliance.
• Build and maintain strong investigator site relationships and data quality.
• Identify and resolve site issues; escalate to protect trial integrity and patient safety.
• Coordinate regulatory affairs, site activation, and startup activities.

Skills

Clinical monitoring

ICH-GCP

Regulatory knowledge

English

Hebrew

Independent work

Travel readiness

Job description

Bring your monitoring expertise to the forefront of innovation. We are looking for a Contractor Clinical Research Associate (CRA) to join our A-team (hybrid). As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, 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.

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. At Allucent we are big enough to deliver and small enough to care. We know all our colleagues by name and work together as a team to make everyone SHINE.

The role

As a Contractor CRA , 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 Israel.

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.
• Activities around regulatory affairs, site activation and study-startup.

Requirements

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 leading monitoring activities in complex trials, ideally in oncology or rare disease with a minimum of at least 5 years’ experience.
• Strong understanding of ICH-GCP and regulatory guidelines .
• Clear and confident communicator in English and Hebrew.
• Comfortable working independently and managing priorities.
• Willingness to travel, as required.

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.

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.”