Senior Clinical Research Director

Sanofi•Cambridge, MA

1d•$236,250 - $393,750•Hybrid

About The Position

Join our Fitusiran Clinical Team as Senior Clinical Research Director, where you will serve as the primary Clinical Lead for the fitusiran registrational development program and ongoing global regulatory submissions. Qfitlia® (fitusiran) is a first-in-class antithrombin-lowering therapy approved in the United States and multiple countries for the prophylactic treatment of adults and adolescent patients with hemophilia. We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world. 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.

Requirements

Medical Doctor or equivalent with specialist training in Hematology, Internal Medicine, Pediatrics, or other relevant specialty
Minimum 8 years experience
Strong scientific and clinical background with deep understanding of the therapeutic field
Expertise in clinical development and methodology of clinical studies
Understanding of pharmaceutical product development and life cycle management
Excellent communication, problem solving and decisions making skills for interactions across functional areas and for interactions with key regulatory agencies.
Strong leadership and collaboration abilities, including the capacity to inspire and guide cross functional teams towards achieving project and team goals.
English fluent (spoken and written)

Nice To Haves

MD/PhD degree

Responsibilities

Develop and implement clinical development plan strategies.
Lead, support, and oversee the execution of clinical development and study activities.
Collaborate with functions to ensure a uniform, aligned operational approach. Provide leadership, build consensus, and coordinate action plans with other CRDs and stakeholders to resolve project-related clinical study issues.
Contribute to the clinical part of submission dossiers for projects, including responsibilities related to regulatory and safety documents and meetings.
Serve as the medical reference in the team, ensuring the medical relevance of clinical data.
Lead scientific data evaluation and dissemination.
Ensures strict compliance with current regulations, laws and HA guidance as well as with Sanofi’s policies and procedures.
Foster a collaborative, engaging, and high-performing team environment for Clinical Research Directors and Clinical Scientists.