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:Global Study Manager

• Location: France – Marcy l’Etoile

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 Clinical Study Management Team as a Global Study Manager (GSM). You’ll represent and support the Global Clinical Department at the study level.

GSM coordinates Clinical teams with the Global Clinical Development Scientific Expert Leader (GCDSE), managing study timelines, budgets, and quality, and integrating study risks while maintaining operational consistency. Collaborating with all Clinical functions, you’ll optimize deliverables, considering all efficiencies to be gained.

Additionally, you’ll provide assumptions for site numbers and enrollment rates for budget and planning purposes, ensuring accurate reporting and study delivery to upper management.

Main responsibilities:

• Oversees Study management at the Clinical team level about timelines, budget, and risk management
  • Monitors study planning (functional Gantt chart) 
  • Prepares and monitors the investigational trial budget
  • Coordinates identification, monitoring & mitigation of study risks
    
• Drives Clinical team delivery and monitors progress toward Clinical Key Milestones, in alignment with project and study plans and objectives
  • Is responsible for the management of information and timelines within the clinical team. He/she works in close collaboration with the Clinical Operation Lead to ensure alignment of clinical trial activities within the project
    

About you

Education:

• MS in Health or Natural Sciences or equivalent qualification/experience
  

Knowledge:

• 6+ years experience in clinical research/Clinical trial, experience in vaccinology is a plus
• Formal training in GCP methods and knowledge of Code of Federal Regulations (US) and other regulatory agency documents
  

Soft and technical skills:

• Demonstrated interpersonal skills (ability to work with individuals at different levels), team and negotiation skills, resourcefulness (ability to find solutions to operational problems)
• Strong results orientation, project management experience required
• Leadership in a multicultural environment
  

Languages:

• Fluent English communication skills, verbal and written

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
• Play an instrumental part in creating best practice within our manufacturing facility