At Excelya, we combine passion, scientific excellence, and collaboration to support our clients throughout the entire drug development lifecycle. We encourage our employees to be bold, take initiative, and unlock their full potential in an international, fast-growing environment.

We are currently looking for a Quality Assurance Pharmacist to strengthen our Quality team and support pharmaceutical quality systems, product quality activities, and regulatory compliance initiatives.

Key responsibilities :

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.

Working within a global cross-functional environment, our Market Access & International Pricing Consultant will collaborate with Market Access, Finance and local affiliates to ensure accurate pricing data, support strategic planning and contribute to market access initiatives.

Key Responsibilities:

• Manage and maintain international pricing databases across multiple markets.
• Analyze pricing structures, net pricing mechanisms, discounts, rebates, and commercial agreements.
• Perform pricing data reconciliation and quality control activities.
• Support budgeting, forecasting, and financial planning exercises.
• Consolidate and analyze pricing-related financial data.
• Produce reports and insights for Finance and Market Access stakeholders.
• Conduct data audits and cleansing activities to ensure data integrity.
• Collaborate with local affiliates on pricing and reimbursement topics.
• Contribute to the enhancement of pricing processes, methodologies, and tools.
• Support selected Market Access projects, strategic analyses, and launch preparation activities.

Requirements

About Excelya

At Excelya, we combine passion, scientific excellence, and collaboration to support our clients across the entire drug development lifecycle. As a trusted partner of leading pharmaceutical and biotechnology companies, we are looking for a Pharmacovigilance Case Processing Officer to join a global safety team and contribute to the delivery of high-quality pharmacovigilance activities in an international environment.

Missions

As a Pharmacovigilance Case Processing Officer, you will support the Global Safety team and ensure the timely and compliant management of case processing activities.

Your main responsibilities will include:

Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role offers an exciting opportunity to join an Oncology Clinical Science team supporting an ongoing Phase I/II solid tumor clinical study evaluating targeted therapies, immunotherapies, and chemotherapy combinations. You will provide scientific oversight, contribute to patient-level data review, support study deliverables through database lock and Clinical Study Report (CSR) activities, and collaborate with cross-functional teams to ensure high-quality study execution.

Key Responsibilities

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 Administration and Facilities. 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.

The Facilities, Property & Workplace Manager France is accountable for providing safe, functional, cost-effective and welcoming workplaces across Excelya’s French locations.

The role manages facilities operations, workplace services, property coordination and management where necessary, suppliers, budgets and workplace improvement projects. It defines sustainable workplace standards and coordinates internal stakeholders to deliver consistent employee and visitor experience.

Main Responsibilities

-Facilities and workplace operations:

Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role offers an exciting opportunity to join a dynamic and ambitious team. As a Biomarker Assay Strategy Leader, you will drive biomarker assay implementation from late research stages through Proof of Concept (PoC) and beyond, ensuring alignment with biomarker plans and project objectives across the drug development lifecycle.

Key Responsibilities

We are seeking an experienced Clinical Project Manager to oversee and coordinate clinical activities in pharmaceutical environment.
The role involves managing operational aspects of clinical trials, ensuring compliance with regulatory requirements, and acting as the primary interface between local stakeholders, investigators, vendors, and global teams.

This position requires strong autonomy, rigor, and excellent communication skills, with the ability to navigate cross‑functional environments.

Key Responsibilities :

1. Study Management

• Lead and coordinate clinical trial activities at the local level from start‑up to close‑out.
• Ensure local execution of global study plans in alignment with timelines and quality standards.
• Serve as the key point of contact for local investigational sites and regional stakeholders.

2. Regulatory & Compliance Oversight

• Ensure that clinical trial activities comply with local regulations, ICH‑GCP, and internal SOPs.
• Coordinate local submissions to competent authorities and ethics committees when required.
• Monitor adherence to regulatory timelines and manage any corrective actions.

Rejoignez Excelya, CRO internationale accompagnant les entreprises pharmaceutiques, biotechnologiques et de dispositifs médicaux dans leurs projets de développement clinique.

Nos équipes interviennent tout au long du cycle de vie des études cliniques, depuis la conception des protocoles jusqu'au rapport final, grâce à des solutions Full Service, Functional Service Provider (FSP) et Resourcing.

À l'occasion du Forum Emploi des Industries de Santé 2026, organisé le 8 octobre au Palais de la Bourse à Lyon, nous souhaitons rencontrer de nouveaux talents et découvrir vos parcours, vos compétences et vos aspirations professionnelles.

Nos domaines d'expertise

Vous seriez amené à intervenir dans les domaines suivants :

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.

We are seeking a Clinical Outcome Assessment (COA) Lead to drive COA strategy across innovative clinical development programs, ensuring the patient voice is integrated into clinical research and that meaningful outcomes are used to demonstrate the real impact of treatments on patients' lives.

Key Responsibilities:

• Define and lead the COA strategy across clinical development programs.
• Ensure the patient perspective is incorporated into study design and endpoint selection.
• Select, develop, and validate appropriate COA instruments (PROs, ClinROs, ObsROs, PerfOs).
• Provide scientific expertise on patient-centered outcomes and endpoint strategy.
• Collaborate cross-functionally with Clinical Development, Medical Affairs, Biostatistics, Regulatory Affairs, HEOR, and external vendors.
• Support regulatory submissions, publications, and scientific communications related to COA data.
• Oversee COA implementation and data quality throughout clinical studies.

Requirements

Rejoignez Excelya, où Audace, Bienveillance et Énergie sont au cœur de notre façon de travailler. Nous croyons en des solutions innovantes et en un environnement inclusif où collaboration et développement professionnel vont de pair.

Dans le cadre d’un projet stratégique dans l’industrie des dispositifs médicaux, nous recherchons un(e) chef de projet pour accompagner l’industrialisation et la validation d’un procédé de revêtement antithrombotique.

Le/La candidat(e) retenu(e) sera responsable de la gestion et de la validation du procédé de revêtement antithrombotique.  

Il/ Elle sera en charge de transformer les concepts issus de la R&D en procédés industriels robustes, fiables et conformes aux exigences réglementaires et qualité (ISO 13485, FDA, MDR).  
La définition, la mise en place et la validation des moyens de production nécessaires (équipements, procédés) ainsi que leur pilotage et l’amélioration continue afin de garantir la performance industrielle (qualité, coûts, délais).

Missions :

Coordonner une équipe projet composée de 3 à 4 collaborateurs pour mener à bien les missions suivantes :