Clinical Research Associate II
Enregistrez cette offre et organisez votre recherche
Créez un compte gratuit pour enregistrer des offres d'emploi, créer des alertes et revenir à cette liste depuis votre tableau de bord.
Clinical Research Associate II / Senior Clinical Research Associate (France)
Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA II) or Senior Clinical Research Associate (Sr. CRA) to join our A-team. As a CRA II / Sr. CRA at Allucent, you will independently control and monitor investigational sites, pro‑actively detect issues, and 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. This position can be either office based (Paris) or remote.
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.
The role
As a CRA II / Sr. CRA, you will take the lead on monitoring activities, own your sites and relationships with investigators, and be the bridge between sponsor and site. You will mentor junior team members and contribute to our success. Travel throughout France is required.
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.
- Mentor and support junior CRAs, sharing knowledge and best practices.
Requirements
- Experience leading monitoring activities in complex trials, ideally in oncology or rare disease, with a minimum of 2 years as an independent site monitor.
- Strong understanding of ICH‑GCP and regulatory guidelines.
- Clear and confident communicator in English and French.
- Comfortable working independently and managing priorities.
- Willingness to travel in France as required.
Benefits
- Competitive salaries and a comprehensive benefits package.
- Departmental study/training for furthering professional development.
- Mentoring opportunities.
- Internal growth opportunities and career progression.
- Financially rewarding internal employee referral program.
- Eligibility for internal employee recognition programs.
- Eligibility for the Loyalty Award Program.
About Allucent
Our mission is to help bring new therapies to light. At Allucent, you will apply your unique skill set, expertise, and knowledge to build partnerships with our clients as they develop new, life‑improving treatments.
Apply now
If you are interested in this role, please apply through the button or reach out to Yael Kokernoot.
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. Unsolicited resumes sent to Allucent employees will not obligate Allucent to future employment of those individuals.