Clinical Research Associate France H/F Allucent
- Paris - 75
- CDI
- Industrie Pharmaceutique • Biotechn. • Chimie
- Exp. 2 ans min.
À noter sur ce job
Ce poste comporte des spécificités à connaître avant de postuler.
- Willingness to travel, as required (8 DOS per month)
Les missions 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 . 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 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.
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.
Le profil recherché
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 .
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.
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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).
Bienvenue chez Allucent
Allucent Clinical Research Organization™ is on a mission to help bring new therapies to light by solving the distinct challenges of small and mid-sized biotech companies. We're a global provider of comprehensive drug development solutions, including consulting, clinical operations, biometrics, and clinical pharmacology across a variety of therapeutic areas. With more than of experience in over 60 countries, our individualized partnership approach provides experience-driven insights and expertise to assist clients in successfully navigating the complexities of delivering novel treatments to patients. Allucent nurtures a high-performance culture in which we provide continuous training and put emphasis on personal and organizational development and opportunities, anchored by a commitment to high-quality and personalized customer service. We consider effective, frequent, and open communication a key component of developing strategies to meet your needs and goals. We provide lean project management to accomplish operational excellence in terms of timelines, quality, and costs.
Publiée le 21/10/2026 - Réf : ec24bce1-2570-4348-bf99-4c6f894e0ef6
