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.
Job title: Senior Medical Writer
- Location: Marcy l’Etoile
- Job type: Permanent, Full time
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 Medical Writing Team as a Senior Medical Writer and you’ll contribute in coordinating and writing the clinical documents and registrations dossiers.
We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. 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.
Main responsibilities:
- Write clinical documentation according to company guidelines and international government regulations and present clinical data objectively in a clear, concise format.
- Provide scientific knowledge, analytical skills, and insight to Clinical Teams, and contribute to Submission Task Force meetings and cross-functional working groups as needed to facilitate the preparation of clinical documents and registration dossiers.
About you
Mandatory experience:
- At least 2 to 3 years of medical writing experience in Vaccines Clinical Development, within a pharmaceutical company or clinical research organization (CRO).
- Professional background documenting an excellent understanding of and experience in clinical development including clinical study performance/methodology/ basic statistics and/or the regulatory environment.
Soft skills:
- Excellent interpersonal and leadership skills to work both autonomously and collaboratively with transversal teams in a multicultural, multilingual, and geographically dispersed environment.
- Must be deadline oriented, able to work under pressure and with a sense of urgency.
Technical skills:
- Ability to interpret clinical data clearly, accurately, and concisely to summarize and write clinical documentation, including complex submission-level regulatory documents in English.
Education:
- Advanced scientific degree, Master or PhD in life sciences, PharmD, or medically qualified is preferred.
Languages (Mandatory):
- Native English speaker or with proven excellent spoken and written English.
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.
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