Description du projet et contribution du stagiaire/de l’apprenti au projet :
L’entreprise : Historiquement spécialistes de la lutte contre la douleur et de l’automédication, les laboratoires UPSA (Union de Pharmacologie Scientifique Appliquée) ont été créés à Agen en 1935 par le Docteur Camille Bru. Intégrée dans le groupe Bristol-Myers Squibb depuis 1994, UPSA est aujourd’hui à la fois une société et une marque. Depuis plus de 80 ans, UPSA a développé une forte expertise en Europe dans la douleur, l’état grippal, la vitalité, la digestion et la qualité du sommeil.
A travers sa gamme d’automédication, UPSA développe et met à disposition des médicaments, dispositifs médicaux et compléments alimentaires pour traiter les maux du quotidien. Avec plus de 1 500 collaborateurs en France dont plus de 1 200 sur son site industriel d’Agen, UPSA est le 1er employeur privé du Lot-et-Garonne.
A l’échelle internationale, UPSA est présent dans près de 60 pays, principalement en Europe, en Afrique et en Asie. Pour en savoir plus, www.upsa.com .
Période de stage / contrat
Type : Contrat d’apprentissage ou de professionnalisation
Suivi de budget du département par produit : création sub-tactic correspondant au budget approuvé, mise à jour ponctuelle pour les projections du budget, réajustement, suivi des dépenses, Fermetures des PO, utilisation des différents outils SAP – RPM, SRM, Production, ARIBA : DA, Contrats, Créations fournisseurs)
Intégration de nouveaux collaborateurs
En relation régulière avec les assistantes des différentes équipes : marketing, vente, support, …
Qualités requises : Rigoureux, adaptable, volonté de grandir dans une organisation en pleine évolution, capacité à gérer/travailler sur plusieurs sujets en même temps, sens de l’organisation et capacité de priorisation, bonne communication à l’écrit et à l’oral.
Pharmaceutical Meetings Management is one of the fastest growing capabilities. The EMCoE team are an expert on the end to end Health Care professional interactions and meetings management process. Close alignment to the Commercial Business within the local market is crucial in addition to supporting training and resources specific to Meetings Management across the multi-disciplinary team.
Efficient meetings management and speed with HCP payments by the EMCoE team will enable incremental business performance through empowerment of the team to simplify processes, technologies and develop local innovative solutions that will enhance the overall customer experience (both internal and external) at BMS meetings and events. By demonstrating a strong value proposition to the Commercial business EMCoE will be able to deliver sustained long term operational cost savings without compromising efficiency.
MAJOR DUTIES AND RESPONSIBILITIES
Support to implement the strategic imperatives set by WWC HCP Meetings and Congresses.
Work in capability team to develop and optimize the innovative digital solution for China new operation model implementation, both for internal and external platforms
Work on integration and maintain of multi-system with a clear platform management chart and execution plan, and drive agencies to achieve every target progressively.
Responsible for implementation for continuous improvement with standardization, process simplification and automation to elevate the customer experience.
Support on Process optimization transaction, by translating the business request into technology improvements.
Support on internal Event management effectiveness tool building and optimization, by working closely with EMCoE operation team, to understand internal needs.
Facilitate the training and Q&A support for the digital platforms and tools to internal and external users.
Cooperate with MCM team, internal customers, and manage third party vendors.
Track all the event data and Monitor execution results & evaluate effectiveness
Design and improve the standard data report from the digital tracking raw data, to integrate into RF and keep transparency with Global data monitor team
Generate Event dashboard, and analyze data to develop insights and KPI measurements to facilitate execution of long term business plans and growth.
KNOWLEDGE, SKILLS, and COMPETENCIES:
Bachelor degree is required. Technical or consulting background is preferred
At least 4 years working experience in digital relevant field or business operation/event management. Ability to manage the project and process optimization.
Data analysis experience and capability of analytics
Experience on digital platform management and multi-platform integration.
Digital consulting analytics experience is preferred.
Ability to handle multi-task work and strong interpersonal skills
Fluency in English. PMP certificate is preferred
Functional / Technical
Demonstrated ability to work independently and effectively in an internal and external matrix environment, with strong interpersonal and influencing skills
Excellent written and verbal communication to facilitate relationships with peers and management
Demonstrated ability to apply strong quantitative and analytical skills to provide business solutions with a customer-centric focus
Demonstrated ability to Influence others to adhere to Company’s policies and procedures and to take actions; especially those over which there is no formal authority
Solid experience in fast paced business environments
Opportunity to learn and improve the Meetings & Events channel to achieve the WWC and local market business strategy.
Opportunity to share, learn and collaborate amongst the World Wide Commercialization team
Opportunity to be part of an energizing, innovative and supportive culture with colleagues located in the markets, Capability Centers and in HQ.
Opportunity to directly impact customer experience and development of resources
Opportunity to develop an expert understanding of the changing healthcare environment and the customers within it
Opportunity to learn program management such as demand management (who uses the service), performance management (do they like the service) and continuous improvement (what should be done to improve)
To conduct Good Clinical Practice (GCP) and pharmacovigilance (PV) audits, of investigator sites, vendors, partners and internal systems. To act as project-specific liaison between GQRC-CT&S and key stakeholders, including Global Development Operations and Global Regulatory and Safety Sciences personnel, monitoring the status of the projects to plan audits and assuring GQRC-CT&S leadership is informed. To host CFDA inspections at investigators sites and in-house.
Bristol-Myers Squibb Pharmaceutical Research Institute
In Vivo Pharmacology - Senior Research Scientist
Princeton LVL - NJ
This Senior Research Scientist will be conducting a wide range of preclinical in vivo studies of the immunological mechanisms of novel pharmacological agents in the areas of autoimmunity and immuno-oncology drug discovery. Looking for previous extensive hands-on experience with various models of autoimmunity and immunological mechanisms. The qualified candidate will possess the ability to work in a team environment to support preclinical drug discovery programs from target identification/validation through IND enabling activities.
Job Responsibilities and requirements
Extensive and diverse hands-on experience with various preclinical in vivo models of rheumatoid arthritis, inflammatory bowel disease, lupus and immunological pharmacodynamic responses, with excellent skills in rodent dosing and tissue collection. Previous experience in animal imaging is a plus.
Ability to independently design, coordinate and execute in vivo studies. Excellent communications skills with ability to effectively communicate both oral and written scientific results.
Organized and disciplined about record keeping, with proficiency in Microsoft Office. Experience with ex vivo analyses (e.g., primary cell and tissue explant cultures and ELISA) would also be of value.
Willing to split weekend and holiday hours with peers on a rotational basis.
Ability to multitask and meet deadlines in a fast-paced drug discovery environment
Strong organizational skills, motivated to excel, attentive to detail. Dedication to working in a team-oriented environment to contribute to shared project and organizational goals.
B.Sc. or M.S. in the Biological Sciences or closely related field with a minimum of 12 years’ experience, preferably within the Pharmaceutical/Biotechnology sector.
We are seeking a qualified PhD level scientist to join the Computer-Assisted Drug Design team at Bristol-Myers Squibb. In this role, the selected candidate will use computational chemistry methods to drive therapeutic projects from target ID through candidate nomination.
Major Skills Required
PhD required plus 2-8 years of experience
In-depth knowledge of computer-aided drug design, computational chemistry, cheminformatics, bioinformatics or computational biology
Experience using modern methods to drive molecular design hypotheses
A history of impact using computational approaches to drive scientific experiment and design
Strong knowledge of chemical and protein structure and sequence
Background in methods for statistical analysis, cheminformatics, bioinformatics, machine learning or data visualization
Competency in programming and/or scripting would be advantageous (e.g. Python)
An aptitude and desire to learn and apply new techniques is expected
A basic knowledge of medicinal chemistry, biology and ADMET/PK
Personal attributes of integrity, creativity, problem solving, and strong work ethic
Ability to work within a multidisciplinary team across geographic areas to advance discovery projects
Ensure the achievement of demand generation goals through medical promotion, conducting periodic visits to doctors in clinics and hospitals; - Marketing Portfolio Presentation to recent research findings , clinical data product update and delivery of materials with relevant information defined in the marketing plan; - Relationship with non-medical areas (pharmacy , shopping , etc.) to monitor the medical claim ; - Regularly participate in training offered by BMS , conventions and relevant management meetings to the area of activity or product represented ; - Coordinate and monitor events and actions of Marketing in their regional area of operation with clients and doctors; - Respect the compliance rules established by the BMS to relationships with physicians and other stakeholders.