Clinical Scientist R&D Oncology H/F - Excelya

Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions guided by our values Energy, Care and Audacity.

Founded in 2014 and headquartered in Paris, France, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas.

We take a one-team approach to work : our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.

Excelya is committed to helping our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together.About the Job

Join Excelya, whereAudacity, Care, and Energydefine 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 Medical Affairs. 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.
- BE part of the Early Clinical Development team, alongside Clinical Leaders and Clinical Scientists.
- Serve as the medical-scientific reference within the Study Team and Clinical Subteam.
- Work in close collaboration with the Clinical Leader on the assigned study.
- Contribute to the design of clinical studies and to the preparation of clinical documents such as protocols, informed consents, amendments, and study reports.
- Participate in the preparation and annual update of core documents like Investigator Brochure, DSUR, and Risk Management Plans.
- Oversee the management of expert committees (e.g., Data Monitoring Committee, Advisory Boards), including contracts and budgets.
- Support training of internal and external teams on the medical-scientific content of clinical protocols.
- Anticipate and address issues related to patient population, safety, and efficacy data to ensure study milestones are met.
- Support data interpretation and contribute to additional analyses in collaboration with data management, statistics, and clinical operations.
- Contribute to the communication of clinical results through internal meetings, investigator calls, congresses, and publications.
- Participate in the preparation of audits and regulatory inspections.
- May contribute to the development of long-term clinical development plans.

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'sleading mid-size CROwith thebest employee experience. Ourone-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 caremeans 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

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 :avoid requiring minimum years-talent matters most to us !
- Skills :Strong scientific project management skills and experience in cross-functional/matrix environments, Proven ability to lead and mobilize teams, and manage multiple topics simultaneously in a dynamic environment, Excellent communication, scientific synthesis, and problem-solving skills.
- Education :PharmD or PhD in Life Sciences (Biology), with experience in clinical development in oncology
- Languages :Proficiency inFrench & English