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Sr Clinical Research Associate Contractor (France)

FranceFrance·ParisPart-timesenior
HealthcareClinical Researcher
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Quick Summary

Key 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,

Technical Tools
HealthcareClinical Researcher

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.

Responsibilities

~1 min read
  • →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

~1 min read

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.

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.

*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.”

Location & Eligibility

Where is the job
Paris, France
On-site at the office
Who can apply
Open to applicants worldwide

Listing Details

Posted
October 2, 2026
First seen
October 2, 2026
Last seen
October 2, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
67%
Scored at
October 2, 2026

Signal breakdown

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Sr Clinical Research Associate Contractor (France)