Global Medical - Lifecycle Management Lead - Respiratory, Al
Company: Sanofi
Location: Bridgewater
Posted on: February 25, 2021
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Job Description:
The health and safety of our employees and candidates is very
important to us. Due to the current situation related to
the--Coronavirus (COVID-19), we're leveraging our digital
capabilities to ensure we can continue to recruit top talent. As
your application progresses, you may be asked to use one of our
digital tools to help you through your recruitment journey. If so,
one of our--colleagues will explain how these tools will be used
throughout the recruitment process and will be on hand to answer
any questions you might have. Global Medical - Lifecycle Management
Lead - Respiratory, Allergy, & GI From Research and Development to
Sales and Marketing, Sanofi offers a wide range of possibilities.
Discover our open positions and become a health journey partner. Do
you have what it takes for a successful career with Sanofi? Sanofi
is recruiting a new Global Life Cycle Management (LCM) Director,
Airway Medical to support product development through medical
strategy and guidance for Dupilumab in the Global Immunology
Franchise for the asthma indication. Dupilumab has the potential to
change the landscape of asthma treatment and management and to be
part of a paradigm shift. The new Leader will report directly into
Vice President and Head, Global Medical, Respiratory Allergy & GI
and will be responsible for medical activities from Phase III
development through post-launch activities.
With guidance from the Head, Global Medical, Airway, the new leader
will be an integral part of building the Global Medical strategy in
line with the brand strategy supporting development and preparation
for the launch of Dupilumab for airway indications in partnership
with Regeneron. The exceptional new hire will either have strong
LCM expertise or clinical development expertise in respiratory
diseases or a desire to work in the respiratory/pulmonary space
with a solid working knowledge and background in medical
affairs.
A summary of responsibilities includes:
--- Lead the development of the LCM portion of the yearly Global
Medical Plan, making sure the LCM strategy is aligned with the
identified strategic imperatives and data gaps.
--- Managing 2-3 direct reports
--- Provide input into novel life cycle management opportunities
for dupilumab in Phase IIIb and ensure Investigator Sponsored
Studies (ISS) areas of interest are consistent with strategic
objectives for dupilumab
--- Communicate product life-cycle management strategy to
regional/local Medical team members and cross-functional team
--- Responsible for IIS study concept review and approval from GMA
perspective. Ensure that appropriate processes are followed for
review, approval, management and support of studies while
maintaining investigator independence
--- Ensure that studies planned by regional and local affiliates
fit into the global product strategy
--- Establish a strong network within the MA organization (Global,
Regional and local) and also with other stakeholders including
R&D, Clinical Sciences & Operations (CSO), and
Pharmacovigilance teams
--- Ensure and oversee the planning, execution and reporting of
clinical studies as defined in the Global Medical plan and in
accordance with established budgets and timelines. Monitor
performance of phase IV activities (e.g. value creation) from
conception through publication of clinical study results and take
corrective actions or escalate issues as appropriate. Contribute to
continuous improvement of phase IV study related processes and best
practices
--- Responsible for financial management and reporting requirements
of LCM studies, ISSs, other Medical activities with accurate and
timely data and assumptions to support budgeting, forecasting and
long-range planning for the business unit
--- Ensure a patient-centric approach to development of medical
strategy both for product and device development as well as
possible services which can enhance the value proposition of the
product; Provide relevant feedback to market access teams to ensure
optimal pricing and reimbursement strategy and inclusion of
relevant endpoints in clinical trials
--- Serve as primary liaison between Global Medical, Health
Economics and Value Access, Outcomes Research and Real-World
Evidence teams to develop and execute evidence generation plans
--- Establish and maintain strong relationships with experts in the
respiratory field, academics and professionals and/or patient
associations. Prior knowledge of and established relationships with
key opinion leaders in asthma considered an asset--
--- Collaborate with alliance partners at Regeneron and within
Sanofi-Genzyme; take a team-oriented approach to making sure
strategy is clearly defined and consistent with relevant
stakeholders in Research and Clinical Development, New Product
Planning, Commercial, Business Development, Health Economics and
Value Access, Outcome Research and Product Management Functions
--- Travel required, comprising up to 30% Basic Qualifications:
--- MD required--
--- Minimum 5 years' experience in industry medical affairs and/or
clinical development/ academic research
--- Prior experience in a Global or at least Regional Medical
role
--- Prior experience in Immunology/Immuno inflammation Medical Life
Cycle Management--
--- Experience working within an international company with a
complex organizational environment; able to operate in a matrix
team-oriented structure
--- Prior experience in managing a team--
Preferred Qualifications:
--- Global experience highly advantageous
--- Experience in Medical with Respiratory Biologics highly
advantageous
--- Able to work on projects in coordination with the Alliance
partner and establish excellent working relationships and
credibility
--- Excellent communication and presentation skills with the
ability to present scientific data in a credible manner.
--- Able to interface professionally with a wide spectrum of
internal and external academicians, agencies, and industry
executives in the scientific/medical arena
--- Strong understanding of the pharmaceutical/biotech drug
development and commercialization process
--- Leadership skills; personal style that includes a sense of
urgency, as well as flexibility and ability to respond to rapidly
changing environments and circumstances
--- Collaborative and proactive, with a hands-on, roll-up-the
sleeves style and attitude
--- Highest integrity; committed to ethics and scientific standards
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-- 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.
Join our Talent Network and get Sanofi communications delivered to
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Keywords: Sanofi, Trenton , Global Medical - Lifecycle Management Lead - Respiratory, Al, Executive , Bridgewater, New Jersey
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