Director, US Regulatory Affairs - Advertising and Promotion
Company: Sanofi EU
Location: Cambridge
Posted on: May 23, 2025
Job Description:
Job Title: Director, US Regulatory Affairs - Advertising and
PromotionLocation: Cambridge, MA or Morristown, NJAbout the jobAre
you ready to shape the future of medicine? The race is on to speed
up drug discovery and development to find answers for patients and
their families. Your skills could be critical in helping our teams
accelerate progress.We are an innovative global healthcare company
with one purpose: to chase the miracles of science to improve
people's lives. We're also a company where you can flourish and
grow your career, with countless opportunities to explore, make
connections with people, and stretch the limits of what you thought
was possible. Ready to get started?Main Responsibilities:
- Makes decisions, provides direction and oversight for the
day-to-day activities for assigned products, departmental
activities, and direct reports.
- In conjunction with the Sr. Director/Product Support Head,
imparts senior regulatory guidance and advice during issues
management activities; provides oversight and guidance for Rapid
Response Teams; functions as the therapeutic product expert for
Region NA, A&P.
- Continually monitors the regulatory environment, interprets new
regulations, guidance's, and enforcement activities/trends and
evaluates the impact on external environments and the
business.
- Develops and implements regulatory strategies for marketed
products within their product area and mentor and develop others in
executing strategy.
- Establishes and develops key internal relationships with
therapeutic product leaders in R&D and Corporate to foster open
communication and teamwork.
- Assures alignment and consistency in Region NA, A&P policy
application within and across therapeutic products; takes into
account the totality of product-related and company
activities.
- Assists in ensuring product support relationships with FDA are
established and maintained.
- Provides input into the global organization for labeling
strategies of marketed drugs. Demonstrates significant autonomy in
carrying out assigned duties and responsibilities.About
YouExperience:
- 8+ years of experience within pharmaceutical or medical device
Regulatory Affairs
- Successful track record of relevant advertising & promotion
regulatory experience
- Dealt effectively with cross-functional groups, which may
include Medical, Legal, Marketing, etc.
- Experience managing others is preferredEducation:
- Minimally, possess a Bachelor's degree from an accredited
four-year college or university in a relevant Life Sciences
discipline or specializationAdditional Skills:
- Understanding of the U.S. pharmaceutical marketplace and
familiarity with medical terminology. Understands issues, problems,
and opportunities by comparing data from different sources to draw
conclusions and then can choose a course of action or develop the
appropriate solution.
- Regularly demonstrates the ability to participate in a more
strategic capacity in the functional area and day-to-day
decision-making process.
- Extensive knowledge and understanding of complex medical and
scientific subject matter.
- Can build networks to obtain cooperation without relying on
authority. You will also have the ability to work well within
cross-functional teams.
- Generates innovative solutions in work situations, trying
different and novel ways to deal with work problems and
opportunities.
- Shows ability to use appropriate interpersonal styles and
techniques and can modify behavior to gain acceptance of ideas or
plans.
- Able to establish priorities and timelines to effectively
self-manage workload. Is able to multi-task exceptionally
well.
- Deals with people in an honest and forthright manner
representing information and data accurately. -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 it's 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-SA ---#LI-SA#LI-Onsite#vhdAll compensation will be
determined commensurate with demonstrated experience. Employees may
be eligible to participate in Company employee benefit programs,
and additional benefits information can
Keywords: Sanofi EU, Framingham , Director, US Regulatory Affairs - Advertising and Promotion, Executive , Cambridge, Massachusetts
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