Senior Global Medical Director Lead- Upper Airways & Medical Evidence Generation
Company: Sanofi
Location: Cambridge
Posted on: March 19, 2023
Job Description:
Senior Global Medical Director Lead- Upper Airways & Medical
Evidence Generation page is loaded Senior Global Medical Director
Lead- Upper Airways & Medical Evidence Generation Bewerben
locations Cambridge, MA time type Vollzeit posted on Gestern
ausgeschrieben job requisition id R2677814 Senior Global Medical
Director Lead - Upper Respiratory & Medical Evidence Generation
Sanofi is recruiting a new Senior Global Medical Lead to support
product development through medical strategy and guidance for
dupilumab as the Senior Global Medical Lead for Upper Airways
(CRSwNP, AFRS) in the Immunology Franchise (50%) along with heading
up the Medical Evidence Generation team (50%). This role will have
1-2 direct reports over time.Dupilumab has the potential to change
the landscape of TYPE 2 diseases, particularly asthma, nasal
polyposis and eosinophilic esophagitis management & treatment, The
new Senior Global Medical Lead will report directly into Vice
President, Global Medical Affairs, Respiratory Allergy and
Gastroenterology, and will be responsible for medical affairs
activities from late phase III development through post-launch
activities. With guidance from the Vice President, Global Medical
Affairs, Respiratory Allergy and Gastroenterology, the new Senior
Medical Lead will be an integral part of executing the global
medical affairs 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 content area expertise in respiratory
diseases or a desire to work in the respiratory/pulmonary space
with a solid working knowledge and background in medical affairs.
Summary of responsibilities include:
- Support building and execution of the Global Medical Affairs
strategy and plan for CRSwNP for Dupilumab
- Work collaboratively with LCM Lead and ensure synergy of
activities and collaboration for Integrated Evidence Generation
Plan (IEGP) development. -
- Establish and maintain strong relationships with experts (ENTS,
Allergists, Pulmonologists, Gastroenterologists, academics and
professionals and/or patient associations
- Prior knowledge of and established relationships with key
opinion leaders in asthma considered an asset
- Organize and lead advisory boards or roundtables for
anti-IL-4/IL-13 and gain strategic insights for medical,
scientific, and development strategy
- Provide Medical Affairs support to the review of requests for
CME, grants and sponsorships. Ensure that review and approval
processes strictly follow compliance guidelines
- Partner with Scientific Communications in the development of
strategy and content for company-sponsored symposia and education
modules for internal/external training
- Give significant input to publications and co-author relevant
abstracts. -
- Drive process of data dissemination and ensure that it is
publicly presented in an appropriate and timely fashion and in a
fair and balanced manner
- Execute on Medical Evidence Generation plan demonstrating real
world data to support dupilumab use in appropriate patients,
increase scientific share of voice for dupilumab; define and
prioritize the future needs including new study ideas and tactics
to prioritize the best areas for clinical trial investment
- Ensure the scientific integrity of sponsored and supported
research, information, and relationships with healthcare providers
and patient advocacy groups
- 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
- Provide medical support, education and guidance to commercial,
marketing and sales teams -
- Provide medical support to promotional and legal review
committees as needed
- Coordinate the network of affiliate Medical Directors through
regular contacts and meetings
- Collaborate with alliance partners at Regeneron; 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
- Maintain knowledge of asthma marketplace, stay current on
leading edge products development efforts and provide perspective
to the business on the treatment landscape
- Travel required, comprising approximately 20%-30% Basic
Qualifications:
- Advanced degree (e.g. MD/DO, PharmD) ideally a physician is
preferred for this role but if a PharmD then should be combined
with significant industry experience working in related areas (e.g
Global Medical Affairs experience in immunology, HEVA/HEOR, LCM,
Clinical Development), preferably related to Immunology.
- Minimum 8 years' experience in industry medical affairs and/or
clinical development
- Experience working within an international company with a
complex organizational environment and/or with an alliance partner;
able to operate in a matrix team-oriented structure Preferred
Qualifications
- Global medical experience is highly advantageous
- Experience working in alliance environment to establish
excellent working relationships and credibility
- Able to work on projects in coordination with alliance partner,
Regeneron
- 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.As a healthcare company and a
vaccine manufacturer, Sanofi has an important responsibility to
protect individual and public health. All US based roles require
individuals to be fully vaccinated against COVID-19 as part of your
job responsibilities.According to the CDC, an individual is
considered to be "fully vaccinated" fourteen (14) days after
receiving (a) the second dose of the Moderna or Pfizer vaccine, or
(b) the single dose of the J&J vaccine. Fully vaccinated, for
new Sanofi employees, is to be fully vaccinated 14 DAYS PRIOR TO
START DATE.#GD-SG -
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30 Tagen ausgeschrieben About Us Sanofi ist ein weltweites
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Keywords: Sanofi, Cambridge , Senior Global Medical Director Lead- Upper Airways & Medical Evidence Generation, Executive , Cambridge, Massachusetts
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