? High Salary! Director, US Regulatory Affairs - Advertising and Promotion
Company: Sanofi
Location: Morristown
Posted on: June 25, 2025
|
|
Job Description:
Job Title: Director, US Regulatory Affairs - Advertising and
Promotion Location: Cambridge, MA or Morristown, NJ About the job
Are 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 You Experience: - 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 preferred
Education: - Minimally, possess a Bachelor’s degree from an
accredited four-year college or university in a relevant Life
Sciences discipline or specialization Additional 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 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.
Keywords: Sanofi, West Orange , ? High Salary! Director, US Regulatory Affairs - Advertising and Promotion, Science, Research & Development , Morristown, New Jersey