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Senior Medical Writer

Marcy-l'Étoile, France Permanent Date posted Jul. 31, 2024
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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:

This is a position for an experienced medical writer who is able to take full responsibility for the writing of clinical documents, including clinical protocols, clinical study reports, and Investigator Brochures and more complex regulatory dossiers according to company and agency guidelines.

  • He/she writes clinical documentation according to company guidelines and international government regulations and presents clinical data objectively in a clear, concise format
  • He/she provides scientific knowledge, analytical skills, and insight to Clinical Teams, and contributes 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

PursueProgress. 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!

Please provide your resume in PDF format Please provide your resume in PDF format.

#LI-FRA#LI-Hybrid

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 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com

Apply Now
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Sanofi careers in France

We're 20,000 people, working across 28 sites in France with one goal: getting medicines and vaccines to people who need them most. From day one, you'll take on exciting projects to set the course of your career. Whether you're a researcher or a marketer, you'll discover the tools, resources, and support you need to pursue progress. Develop your skills and work in inclusive teams to positively impact millions of people globally.

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