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Sanofi Group Manager, US Regulatory Affairs Oncology in Cambridge, Massachusetts

Position Overview:

This position is based in our Cambridge, MA site and will be responsible for providing US regulatory strategic and tactical support for both development and marketed products for the GBU. In this capacity, the Manager US RA will be responsible for providing US regulatory advice for development programs and marketed products working either independent from or with the US Regulatory Lead, the Global Regulatory Lead (GRTL) and Global Regulatory Team (GRT) (regions, Regulatory CMC, Regulatory Operations, EU authorized representatives, Labeling). The role may be a US Regulatory Lead for products that are early in pharmaceutical development or assigned to perform tasks associated with routine regulatory application maintenance. For projects where the role is assigned as the USRL, person will sit on GRTs.

Key Responsibilities:

  • Support the preparation of regulatory documentation and submission activities to meet business and agency milestones.

  • Create submission plans, manage timelines and document workflow from draft through finalization for US submissions.

  • Prepares routine submissions in compliance with department and regulatory requirements and guidelines. Assists with larger or more complex submissions.

  • Identify risks to timeline and assists the US Regulatory Lead (USRL).

  • Work with USRL and Regulatory Operations to identify resource requirements and strategies to address overlapping resource demands and rate limiting factors.

  • Identify and manage issues and opportunities that impact submissions timelines; ensures appropriate communication, resolution and/or escalation as needed.

  • Ensure regulatory plans are monitored, progress/variance communicated to the USRL and any risks are highlighted.

  • Collaborate within regulatory and cross-functional colleagues on the preparation and submission of regulatory filings, including major marketing applications in the US.

  • Prepare and review sections of regulatory submissions for IND/CTA original submissions and amendments, orphan designations, and pediatric investigation plans.

  • Participate in regulatory research activities, as needed.

Basic Qualifications:

  • BS in pharmaceutical-related scientific field.

  • Minimum 1-3 years of regulatory experience in a biotech/pharma company.

  • Excellent project management and writing skills, as well as a good understanding of the underlying science.

  • Experience with preparation of initial INDs, IND amendments, DSURs and meeting briefing documents. Experience with BLA, NDA, or MAA a plus.

  • Understanding of the development of drugs and/or innovative biologics products. Experience in oncology drugs a plus.

  • Basic understanding of regulations and guidelines related to drug development and registration is required.

  • Ability to work effectively in a collaborative team environment where results are achieved through influence and the incorporation of multiple points of view.

  • Independently motivated, detail oriented and good problem solving ability.

  • Demonstrated ability to handle multiple projects is required.

  • Excellent organizational skills, sufficient to multi-task in an extremely fast-paced environment with changing priorities.

  • Excellent communication skills and ability to influence across multiple functions.

At Sanofi R&D North America, we deliver meaningful solutions for patients. We transform science into breakthrough, best-in-class and first-in-class medicines and vaccines. We believe in creating a diverse and inclusive workforce – and workplace – which brings together the collective brainpower of over 2,000 colleagues and provides you with an exciting place to grow and develop. We set the bar high, and we deliver. Join us and together we will build on our trusted legacy of breakthroughs for society.

As a healthcare company and a vaccine manufacturer, Sanofi has an important responsibility to protect individual and public health.This position will require individuals to be fully vaccinated against COVID-19 as part of your job responsibilities.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.



At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.