Global Project Head, Solid Tumor Immuno-Oncology

About the job

The Global Project Head (GPH) drives worldwide clinical development and life cycle management for a late‑stage Sanofi immunotherapeutic compound within Solid Tumor Oncology. The GPH leads the GPT (global product team) to ensure optimal development of the global compound development strategy in collaboration with the GBT (global brand team). In this assignment the GPH will be accountable for the compound clinical development strategy and execution, with a focus on studies for regulatory purposes and including budget planning.

• Collaborate 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), ensuring correct planning and implementation of end‑to‑end compound strategy.
• Represent the Clinical Development function at the cross‑functional GBT responsible for commercial brand strategy.
• Partner with the PCL to present and discuss development strategy with key internal stakeholders, external investigators, advisory boards, and worldwide regulatory authorities.
• Act as an essential contributor to Sanofi Solid Tumor Oncology and cross‑asset Disease Area strategies.
• Conduct clinical development assessment of external business development opportunities in Hematopoietic Stem Cell Transplantation, and if applicable, become responsible for implementing the development strategy.

About you

• MD or PhD (or equivalent advanced degree in a relevant life sciences discipline)
• 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

Preferred Qualifications

• Experience leading pivotal trials to support submission for regulatory approval in solid tumor oncology
• 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
• Experience in regional alliance partnerships or co‑development

Soft and technical skills

• Strong leadership and clinical expertise in the field, enabling effective international collaboration with external and internal stakeholders
• Ability to integrate new information, adapt and change direction in response to evolving data and/or external landscape (CI, regulatory, etc.)
• Ability to develop strong networks internally and externally
• Strong interpersonal, cross‑functional, and cross‑cultural communication skills
• Ability to define clear and challenging yet realistic goals
• Ability to assess the balance of investment and deliverables
• Results‑ and customer‑focused
• Organizational awareness

Languages

• Excellent written and verbal communication skills in English across cultures, functions, and seniority levels

Benefits

• High‑quality healthcare, prevention and wellness programs
• At least 14 weeks’ gender‑neutral parental leave
• Well‑crafted rewards package that recognizes contribution and amplifies impact

Salary

The salary range for this position is: €114,800.00 - €153,067. Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors.

We provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.