Regulatory Regional Leader
il y a 2 semaines
**About the Job**
Join Excelya, where **Audacity, Care, and Energy** define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.
This role is an exciting opportunity to contribute to a dynamic, ambitious team in Safety. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.
- Develop the regional regulatory strategy and oversee registration processes in alignment with global objectives.
- Ensure that regulatory dossiers comply with all relevant regional regulatory requirements.
- Serve as the main point of contact with Local Regulatory Affairs (LRA) teams.
- Consolidate and validate regional requirements; advise the Global Regulatory Leader (GRL) on specific national regulations.
- Support the preparation of registration files, procedures, and Life Cycle Management (LCM) activities together with the GRL and submission manager.
- Assist in drafting clear and accurate responses to Health Authorities’ questions.
- Provide detailed explanations and context regarding Health Authority queries or feedback.
- Ensure that regulatory databases and tracking systems are updated and maintained accurately.
**Requirements**:
**About You**
At Excelya, **taking audacious steps is encouraged**, so we’re looking for individuals who are ready to grow with us and share our values.
- **Experience**: Experience in regulatory affairs (junior profile with European regulatory experience strongly preferred) (avoid requiring minimum years—**talent matters most to us**)
- **Skills**:Familiarity with regional registration processes, dossier preparation, and interactions with Health Authorities.
- **Education**: Minimum Master**’s degree (Bac +5)** in clinical research or a related field
- **Languages**: Fluency in French & English
**Benefits**
**Why Join Us?**
At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.
Here’s what makes us unique—
We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s **leading mid-size CRO**with the **best employee experience**. Our **one-stop provider service model**—offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient’s journey.
**Excelling with care** means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.
-
RWE & Pharmacoepidemiology Lead
il y a 2 jours
Saclay, France Excelya Group Temps pleinA leading mid-size CRO in Île-de-France seeks an experienced professional to lead pharmacoepidemiology and Real-World Evidence projects. You will ensure scientific quality and regulatory compliance while collaborating with cross-functional teams to enhance patient outcomes. The ideal candidate has strong methodological expertise, experience in RWE, and an...
-
Lead, Safety Periodic Reports
il y a 1 jour
Saclay, France Excelya Temps pleinAn innovative healthcare company in Saclay is seeking a Safety Periodic Reports Lead to oversee the development of safety reports. The role requires a strong background in pharmacovigilance, fluency in French and English, and a relevant Master's degree. Candidates will work in a collaborative environment, contributing to high-quality services and regulatory...
-
Senior Real-World Evidence
il y a 1 jour
Saclay, France Excelya Temps pleinA leading mid-size CRO is seeking a professional to lead pharmacoepidemiology and real-world evidence projects. You will be responsible for ensuring methodological quality and regulatory compliance, conducting feasibility studies, and collaborating with cross-functional teams. The ideal candidate should have substantial experience in pharmacoepidemiology and...
-
Safety Periodic Reports Lead
il y a 2 jours
Saclay, France Excelya Temps pleinSafety Periodic Reports Lead Join Excelya as a Safety Periodic Reports Lead. About the Job Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. This role is an exciting opportunity to lead the...
-
Safety Periodic Reports Lead
il y a 1 jour
Saclay, France Excelya Group Temps pleinAbout the Job Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. This role is an exciting opportunity to lead the development of safety periodic reports within our dynamic and ambitious Safety...
-
Safety Periodic Reports Lead
il y a 6 jours
Saclay, Île-de-France EXCELYA Temps pleinAbout the JobJoin Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.This role is an exciting opportunity to lead the development of safety periodic reports within our dynamic and ambitious Safety...
-
Safety Periodic Reports Lead
il y a 5 jours
Saclay, Île-de-France Excelya Temps pleinAbout the JobJoin Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.This role is an exciting opportunity to lead the development of safety periodic reports within our dynamic and ambitious Safety...
-
Safety Periodic Reports Lead
il y a 5 jours
Saclay, Île-de-France Excelya Temps pleinAbout the JobJoin Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.This role is an exciting opportunity to lead the development of safety periodic reports within our dynamic and ambitious Safety...
-
Regulatory Global Lead Junior/ Responsable Régulation
il y a 2 jours
Saclay, France Ascalium Temps plein**Responsabilités**: - ** Gestion de Dossiers en Oncologie**: Prendre en charge les aspects réglementaires des dossiers en oncologie. - ** Membre de l'Équipe Réglementaire Globale**: Participer activement aux réunions et contribuer à la stratégie globale. - ** Collaboration Interne**: Travailler en étroite collaboration avec les différents...
-
Pharmacovigilance Case Processing Manager
il y a 2 jours
Saclay, France Servier France Temps pleinPharmacovigilance Case Processing Manager (F/M)We are a human-sized, international and independent pharmaceutical group governed by a Foundation. Our mission: to advance therapeutic progress for patients. As a world leader in cardiology, we aim to focus on oncology by 2030, dedicating more than 70% of our R&D budget to difficult-to-treat cancers, while...