About The Position

Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions. About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Requirements

  • MD or PhD
  • 7 or more years of experience in clinical development in Solid Tumor Oncology, in the biotech or pharmaceutical industry
  • Thorough understanding of global drug development and functional roles and responsibilities
  • Proven effective leadership of high-performing cross-functional clinical development teams
  • Experience in successful submissions for marketing authorization
  • Excellent written and verbal communication skills

Nice To Haves

  • Experience leading pivotal trials to support submission for regulatory approval in solid tumor oncology.
  • Strong leadership and clinical expertise in the field, to enable effective international collaboration with external and internal stakeholders.
  • Experience preparing regulatory submissions, and discussion / negotiation with health authorities.
  • Experience collaborating with commercial and medical functions in launch and/or post-launch settings
  • Experience working in a matrix environment
  • Ability to integrate new information, adapt, and change direction in response evolving data and/or external landscape (CI, regulatory, etc).
  • Ability to develop strong networks internally and externally.
  • Experience in regional alliance partnerships or co-development
  • Strong interpersonal, cross-functional, and cross-cultural communication skills
  • Ability to define clear and challenging, but realistic, goals.
  • Ability to assess the balance of investment and deliverables.
  • Results and customer focused.
  • Organizational awareness.

Responsibilities

  • Drives worldwide clinical development and life cycle management for a late-stage Sanofi Antibody Drug Conjugate (ADC) compound within Solid Tumor Oncology.
  • Leads the GPT (global product team) to ensure optimal development of the global compound development strategy in collaboration with the GBT (global brand team).
  • Accountable for the compound clinical development strategy and execution, with a focus on studies for regulatory purposes and including budget planning.
  • Collaborates with the Principal Clinical Lead (PCL) and Global Project Manager (GPM) to lead the cross-functional GPT (which includes translational, regulatory, drug manufacturing, safety, medical and commercial compound leads), to ensure correct planning and implementation of end-to-end compound strategy.
  • Represents the Clinical Development function at the cross-functional GBT responsible for commercial brand strategy.
  • Partners with the PCL to present and discuss development strategy with key internal stakeholders, external investigators and advisory boards, and worldwide regulatory authorities.
  • Essential contributor to Sanofi Solid Tumor Oncology and cross-asset Disease Area strategies.
  • Responsible for the Clinical Development assessment of external business development opportunities in Hematopoietic Stem Cell Transplantation, and, if applicable, become responsible for the implementation of this Development strategy.

Benefits

  • High-quality healthcare
  • Prevention and wellness programs
  • At least 14 weeks’ gender-neutral parental leave

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What This Job Offers

Job Type

Full-time

Career Level

Senior

Education Level

Ph.D. or professional degree

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