Activez les alertes d’offres d’emploi par e-mail !

Alternance - Chef de projet medical

Bristol-Myers Squibb

Rueil-Malmaison

Sur place

EUR 40 000 - 60 000

Plein temps

Il y a 18 jours

Mulipliez les invitations à des entretiens

Créez un CV sur mesure et personnalisé en fonction du poste pour multiplier vos chances.

Résumé du poste

Bristol-Myers Squibb recherche un assistant pour soutenir le Responsable de la Zone Thérapeutique dans des missions variées allant de la qualité des matériaux médicaux à l'exécution d'études cliniques. Ce rôle exige un diplôme scientifique et une connaissance du secteur pharmaceutique. La flexibilité et la capacité à travailler en collaboration sont essentielles pour réussir dans ce rôle où l'impact sur la vie des patients est significatif.

Prestations

Concurrence des avantages et services pour les objectifs personnels et professionnels

Qualifications

  • Diplôme médical ou scientifique requis, de préférence avec doctorat.
  • Connaissance du secteur pharmaceutique et du système de santé français.

Responsabilités

  • Assister le responsable de la zone thérapeutique dans toutes ses missions.
  • Soutenir la communication des données cliniques pour les produits en développement.
  • Contribuer au développement et à la promotion de la filiale France.

Connaissances

Acuité scientifique
Connaissance des pratiques cliniques
Connaissance de l'accès au marché des médicaments
Connaissance des méthodologies d'essai clinique
Connaissance en biostatistiques
Compétences en communication de données scientifiques
Autonomie
Agilité en collaboration interfonctionnelle
Anglais professionnel

Formation

Diplôme médical ou scientifique (Doctorat, Pharmacien, PhD, etc.)

Description du poste

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words typically associated with a job, but at Bristol Myers Squibb, work is anything but usual. Here, interesting work happens daily across departments, from optimizing production lines to breakthroughs in cell therapy, transforming lives and careers. You’ll have opportunities to grow and thrive with high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb values balance and flexibility. We offer competitive benefits, services, and programs to support your personal and professional goals. Read more: careers.bms.com/working-with-us.

  • Assist the Therapeutic Area Manager (DAS) in all their missions and responsibilities.
  • Support the therapeutic area manager to ensure the scientific and medical quality of materials for healthcare professionals and training materials for delegates, in compliance with applicable regulations (Public Health Code, Promotional Information Charter, etc.).
  • Help train and inform delegates on scientific and medical data.
  • Assist in establishing data generation strategies to understand product use in patients.
  • Support communication of clinical data for products in development or on the market.
  • Contribute to the development and promotion of the France subsidiary within the group, collaborating with Global R&D teams to accelerate data generation.
  • Support product strategy and medical actions to aid development, proper use, and patient access.
  • Assist in executing the portfolio of clinical studies (ISR, BMS Sponsored NIR) and collaborate with the Clinical Research Department for successful clinical trials.
  • Monitor and ensure activities stay within budget.

Maintain the highest ethical standards, adhering to quality policies, internal procedures, the Public Health Code, regulations, and hospital-specific rules.

Required Education:

Medical or Scientific degree, preferably with a doctorate (Doctor, Pharmacist, PhD, etc.) or dual qualification (business school, etc.), in progress.

Required Experience:

Knowledge of the pharmaceutical industry, medical environment, and/or the French healthcare system is a plus.

Required Skills:

  • Strong scientific acumen and good knowledge of clinical practices in France.
  • Understanding of healthcare environment and drug market access.
  • Knowledge of clinical trial methodologies and observational studies.
  • Biostatistics knowledge.
  • Ability to communicate scientific data effectively.
  • Autonomous and agile in cross-functional collaboration.
  • Professional English proficiency.

If you find a role intriguing but your resume isn’t a perfect match, we encourage you to apply. You might be one step away from a transformative career.

Unique Work and Career Opportunities
Inspired by the vision “Transforming patients’ lives through science,” every BMS employee plays a vital role in meaningful work. We empower our team to leverage individual talents and perspectives within a supportive culture, promoting global clinical trial participation. Our core values—passion, innovation, urgency, accountability, inclusion, and integrity—bring out the best in everyone.

On-site Protocol

BMS has a structure determining work location: site-essential, site-by-design, field-based, or remote-by-design. The assigned occupancy type depends on role responsibilities:

Site-essential roles require 100% onsite work. Site-by-design roles may qualify for hybrid work with at least 50% onsite. Field-based and remote roles involve travel to meet clients, patients, or partners and attend meetings as needed.

BMS is committed to supporting employees with disabilities through transparent recruitment, accommodations, and ongoing support. Requests for accommodations can be directed to adastaffingsupport@bms.com. Visit careers.bms.com for our Equal Employment Opportunity statement.

We prioritize your well-being and recommend vaccination against Covid-19 and boosters. We consider qualified applicants with arrest or conviction records per applicable laws.

If you reside or plan to work in Los Angeles County, see additional info here: https://careers.bms.com/california-residents/.

All application data will be handled according to privacy policies and regulations.

Obtenez votre examen gratuit et confidentiel de votre CV.
ou faites glisser et déposez un fichier PDF, DOC, DOCX, ODT ou PAGES jusqu’à 5 Mo.