Medical Director - US Rare
Company: Sanofi
Location: Cambridge
Posted on: March 26, 2026
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Job Description:
Job Title: Medical Director - US Rare Location: Cambridge, MA
About the Job Join the team transforming care for people with
immune challenges, rare diseases, cancers, and neurological
conditions. In Specialty Care, youll help deliver breakthrough
treatments that bring hope to patients with some of the highest
unmet needs. Sanofi's US Rare Medical Team is seeking an
exceptional Medical Director to join our mission-driven
organization dedicated to transforming the lives of patients with
rare diseases. This strategic medical affairs role offers the
opportunity to shape medical strategy, drive scientific excellence,
and contribute to breakthrough therapies that address significant
unmet medical needs. The successful candidate will serve as a key
medical expert, providing scientific leadership across multiple
therapeutic areas while collaborating with cross-functional teams
to advance our rare disease portfolio. About Sanofi Rare Diseases
At Sanofi, we are united by a shared purpose: to chase the miracles
of science to improve people's lives. Our Rare Diseases division is
at the forefront of developing innovative therapies for patients
with rare and ultra-rare conditions who often have limited or no
treatment options. We combine cutting-edge science with deep
patient understanding to deliver transformative medicines that make
a meaningful difference in patients' lives. Join us in our mission
to turn science into miracles for the rare disease community. About
Sanofi: Were an R&D-driven, AI-powered biopharma company
committed to improving peoples 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 peoples lives. Main Responsibilities
Medical Strategy & Scientific Leadership Develop and execute
comprehensive medical strategies for assigned rare disease
therapeutic areas Provide scientific and clinical expertise to
support product lifecycle management from late-stage development
through commercialization Lead medical input into strategic
planning Serve as internal medical expert and scientific resource
for assigned therapeutic areas Clinical Development Support
Collaborate with clinical development teams to provide medical
insights for ongoing and future clinical trials Review and provide
medical input on clinical protocols, study designs, and regulatory
submissions Support post-marketing surveillance activities and
real-world evidence generation Contribute to risk management and
pharmacovigilance activities Key Opinion Leader (KOL) Engagement &
External Relations Identify, develop, and maintain relationships
with leading experts and key opinion leaders Plan and execute
advisory boards, expert panels, and scientific meetings Facilitate
scientific exchange and collaboration with external researchers and
clinicians Represent Sanofi at scientific conferences, medical
meetings, and professional forums Medical Information & Scientific
Communications Oversee medical information responses and ensure
accuracy of scientific communications Develop and review medical
education materials, publications, and scientific content Support
preparation of manuscripts, abstracts, and scientific presentations
Ensure compliance with regulatory requirements and company policies
in all communications Cross-Functional Collaboration Partner with
commercial, regulatory, clinical, and market access teams to align
medical strategy with business objectives Collaborate with global
medical affairs colleagues to ensure consistency and leverage best
practices Work closely with field medical team to support
field-based medical activities Contribute to cross-functional
project teams and strategic initiatives About You Required
Qualifications Medical Degree (MD), PharmD, PhD from an accredited
institution Minimum 5 years of experience in US medical affairs
within pharmaceutical industry or biotechnology companies
Understanding of drug development process, and medical affairs
functions Experience in medical launch strategy development and
execution Publication and presentation experience in peer-reviewed
journals and scientific conferences Preferred Qualifications
Clinical or research experience in pulmonology (preferred but not
required) Experience in end-stage clinical development including
Phase III trials and regulatory submissions (preferred but not
required) Experience in rare diseases or specialty therapeutic
areas Previous experience in medical affairs leadership roles Key
Competencies and Skills Scientific & Clinical Excellence Scientific
and clinical expertise in rare diseases and related therapeutic
areas Ability to interpret and communicate complex clinical data to
diverse audiences Strong analytical and critical thinking
capabilities Evidence-based decision-making skills Communication &
Leadership Excellent written and verbal communication skills Proven
ability to present complex scientific information to various
stakeholders Strong interpersonal skills and ability to build
relationships with internal and external partners Strategic &
Collaborative Mindset Strategic thinking with ability to see the
big picture while managing tactical execution Collaborative work
style in cross-functional team environments Ability to manage
multiple priorities simultaneously Patient-centric mindset with
passion for improving outcomes for rare disease patients 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 its 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. 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. GD-SG LI-GZ LI-Onsite vhd All
compensation will be determined commensurate with demonstrated
experience. Employees may be eligible to participate in Company
employee benefit programs, and additional benefits information can
be found here.
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