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Global Safety Officer

Sanofi

Gentilly

Hybride

EUR 65 000 - 80 000

Plein temps

Aujourd’hui
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Résumé du poste

Une entreprise pharmaceutique internationale recherche un Global Safety Officer à Gentilly. Le candidat idéal aura un M.D. et au moins 3 ans d'expérience en pharmacovigilance internationale. Les responsabilités incluent la gestion de la sécurité des produits I&I, la communication avec des partenaires externes et la direction de l’évaluation des risques. Ce poste offre des opportunités de carrière et un environnement de travail collaboratif.

Prestations

Programme de bien-être
Congé parental neutre en genre de 14 semaines
Opportunité de développement professionnel

Qualifications

  • Minimum 3 years' international pharmacovigilance experience for MD, or 5 years for other degrees.
  • Board Certified/Board eligible or equivalent preferred.
  • Proven excellence in similar prior position may substitute for years of experience.

Responsabilités

  • Internal & External Safety Expert for I&I products.
  • Lead Signal Detection & Assessment.
  • Responsible for Risk Assessment & Management.
  • Communicate safety analyses and represent teams.
  • Contribute to Submission Activities.

Connaissances

Excellent clinical judgment
Synthesize and critically analyze data
Communication of complex clinical issues
Risk assessment development
Ability to work under pressure
Leadership in cross-functional teams
Teamwork and interpersonal skills
Fluent in English

Formation

M.D. Degree
Description du poste
Le contenu du poste est libellé en anglais car il nécessite de nombreuses interactions avec nos filiales à l’international, l'anglais étant la langue de travail.

This job offer is accessible to all, regardless of gender.

Global Safety Officer

Location: Gentilly

Main responsibilities:

  • Be the Internal & External Safety Expert for I&I products under development
  • Communicate with and represent PV analyses and PV position within project/product teams, in safety governance and benefit-risk governance activities and committees (e.g. Safety Management Committee, Benefit-Risk Assessment Committee), with external partners, key opinion leaders, and Health Authorities, and during internal and external negotiations
  • Lead Signal Detection & Assessment
  • Be responsible for Risk Assessment & Risk Management & Benefit-Risk Assessment
  • Contribute to Submission Activities
About the job

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. Join our I&I PSPV team as GSO and you’ll be the safety expert for I&I products under development, the top priority of the company, while enjoying lots of opportunities to broaden your experience and hone your skills.

We’re an innovative global healthcare company that helps the world stay ahead of I&I diseases. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.

About you
  • Knowledge & Skills
    • Excellent clinical judgment
    • Capability to synthesize and critically analyze data from multiple sources
    • Ability to communicate complex clinical issues and analysis orally and in writing
    • Able to develop and document sound risk assessment
    • Demonstrates initiative and capacity to work under pressure
    • Demonstrates leadership within cross-functional team environment
    • Excellent teamwork and interpersonal skills are required
    • Fluent in English (written and spoken)
  • Formal Education & Experience Required
    • M.D. Degree
    • For MD, Board Certified/Board eligible, or equivalent, is preferred
    • For M.D., minimum 3 years' and for other degrees, minimum 5 years' total experience in international pharmacovigilance, or equivalent relevant industry experience (e.g. clinical development) with relevant clinical experience considered. Exceptionally, candidates may be considered if they have proven excellence in a similar prior position, even if they have less than 3 years international PV experience
Why choose us?
  • Bring the miracles of science to life alongside a supportive, future-focused team
  • Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally
  • Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact
  • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave
Pursue Progress Discover Extraordinary

Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

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