For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
Vous avez des connaissances scientifiques et souhaitez évoluer dans un rôle alliant expertise scientifique et relation client ?
Nous recherchons un Manager de projets scientifiques F/H en CDI au sein du département du GEMS, spécialisé dans la gestion et la production de modèles transgéniques, sur notre site basé à l’Arbresle (69) dans le nord-ouest lyonnais.
Au sein d’une équipe de 9 personnes, vous serez un interlocuteur central avec les équipes internes et nos clients sur les secteurs France & Europe et aurez un champ d’action transverse selon leurs besoins.
Vous aurez pour responsabilité la gestion de projet de production/amplification de lignées transgéniques dans nos animaleries, mais également des projets incluant des services d’embryologie (FIV, cryopréservation, etc.) – Projets sur des souches transgéniques de souris/rats.
Missions principales
- Identifier les demandes scientifiques des clients, étudier leur faisabilité, participer à leur mise en place.
- Effectuer les devis des projets clients.
- Prendre en charge le projet de la demande client initiale jusqu’à la facturation du projet et cela tout au long de la réalisation du service.
- Assurer la gestion administrative du projet (mis à jour du logiciel de suivi des lignées, saisie des expéditions…).
- Apporter son expertise scientifique pour répondre aux demandes clients et proposer des solutions adaptées.
- Rédiger et transmettre régulièrement les états d’avancement des projets.
Coordonner les acteurs internes et externes pour permettre l’acquisition, la mise en place et le déroulement fluide des projets.
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Profil recherché
- De formation bac +5 ou équivalent, vous avez des connaissances avancées en biologie, avec une expertise fortement recommandée en génétique. Une spécialisation dans un autre domaine tel que l’oncologie, l’immunologie ou tout autre domaine connexe serait un atout.
- Vous avez une expérience professionnelle avérée en gestion de projet scientifiques en interaction directe avec diverses parties prenantes.
- Vous avez un excellent sens du relationnel, capacité à interagir avec des interlocuteurs variés et de bonne capacité d’organisation.
- D’un naturel curieux, avenant et proactif, vous souhaitez rejoindre un environnement scientifique non routinier.
- Vous avez un niveau d’anglais courant, écrit et oral (environnement international quotidien).
- Vous avez une maîtrise des logiciels Excel, Word, Power Point (Logiciel SAP et/ou Salesforce serait un plus).
Modalités
- Poste cadre
- Convention collective de l’industrie pharmaceutique
- Rémunération : à partir de 40 K€ brut annuel sur 14 mois + bonus + intéressement et participation
- Prise en charge de la mutuelle à 60%, restaurant d’entreprise, indemnité de transport, CE
Site non desservi par les transports en commun. Moyen de locomotion indispensable.
About Research Models & Services
Fundamental to basic research and discovery is the use of in vivo models to help identify disease targets and determine potential biological pathways that regulate the condition. As the world’s leader in the production and distribution of the highest quality research animal, with 1 out of 2 animal models produced for preclinical research globally, we understand the importance of this step. With seven decades of experience, our expertise is unmatched, allowing us to provide you with the perfect model, including disease-specific and preconditioned options, for basic research and beyond.
About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
Equal Employment Opportunity
Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to [email protected]. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit www.criver.com.
