Sanofi Group Medical Science Liaison - Respiratory - Central Region (AR, MS, LA, OK, TN) in New Orleans, Louisiana
The Medical Science Liaison (MSL) will be responsible for providing non-promotional scientific, educational, and research support for the Dupilumab – Asthma product in the respective territory. The MSL position is a field-based member of the Medical Affairs team. The MSL should be highly trained in a health care field and well-versed in clinical and for basic science to be able to deliver cutting edge data and technical/practical education to Health Care Professionals (HCP).
This is a remote-based position. The territory for this role includes: AR, MS, LA, OK, TN, The successful candidate must be based in the territory, or willing to relocate there at own cost.
The MSL will be responsible for developing and maintaining relationships with key Respiratory experts and building a well-informed advocacy base for Sanofi Genzyme's Immunology franchise, including compounds in the development program. The MSL will act as a conduit for providing accurate and updated clinical, scientific and medical information to Respiratory Experts, health care professionals, treatments decision-makers and other members of the scientific, provider and payer community (private insurance, payers, medical groups, government agencies, and health systems with drug formularies), in compliance with all relevant company policies.
Maintains business and clinical knowledge of the asthma treatment landscape including current treatment strategies, current and pending competitors, and new therapeutic developments.
Increases Sanofi Genzyme's visibility among leaders in the therapeutic field of Respiratory. Identifies, establishes and maintains collaborative relationships with key Respiratory Experts, investigators, and institutions strategic to product development.
Participates in medical education for healthcare professionals through presentations at office visits, investigator meetings, advisory boards, medical meetings, and other appropriate venues to enhance product and disease state knowledge.
Collaborates with the clinical team and CRA's to coordinate and optimize educational and research support for sites/investigators participating in Sanofi Genzyme's clinical trials.
Responds to unsolicited requests regarding interest in investigator-sponsored studies (ISS), and supports ISS submissions through appropriate internal processes.
Responds to unsolicited request for medical information associated with supported products and disease state areas.
Provides effective clinical presentations to internal and external audiences and tailors presentations to meet the specific needs of the audience (appropriate response to unsolicited requests).
Identifies and communicates key clinical and research issues and insights from industry leaders to appropriate departments to help shape company research, development, and strategies for investigational and commercialized products.
Facilitates the identification of medical community educational needs around Asthma disease state management, including awareness and understanding of appropriate/inappropriate use of company products.
Collaboration with internal and external stakeholders in support of the needs of Key Opinion leaders (KOLs).
Maintains clinical expertise through comprehensive education including attendance at the relevant symposium, scientific workshops, and review of key journals. Participation in required internal training, presentations and journal clubs.
Maintains appropriate communication with Medical, Regulatory, and Legal personnel within the company to ensure appropriate timelines and procedures are met.
Adheres to regulatory and compliance guidelines and company policies in all aspects of scientific dissemination of information to include responses to unsolicited requests for medical information.
Enhances clinical/scientific knowledge of customers and colleagues through education and appropriate scientific exchange.
Works collaboratively with relevant internal stakeholders to identify local/regional educational gaps/needs and apply appropriate field medical support that is aligned with the medical strategy
Provides field updates regarding topics of interest
Addresses administrative and reporting needs on a timely basis or as requested by management.
Travel 60% or greater, including domestic and international travel as needed
Territory: AR, MS, LA, OK, TN
MD, PharmD, Ph.D. or other doctoral-level degree preferred and 2 years related pharma/biotech experience.
Candidates with advanced health care degrees and relevant Respiratory clinical experience consisting of at least 5 years in Respiratory clinical environment may be considered.
Valid driver’s license with a clean driving record and ability to pass a complete background check.
Driving a company car in a safe manner to daily meetings and appointments is required.
Responsible for operating the motor vehicle using safe driving practices, knowledge of and compliance with all company policies, and obeying all traffic laws.
Knowledge and experience in field medical asthma (Respiratory, Immunology) preferred
Knowledge and experience in disease area preferred
Preferred previous pharmaceutical industry experience
Clear understanding of regional medical practice and clinical decision making regards to patient care
Ability to identify the unmet medical, educational, and research needs within the regional medical community
Interpretation of key scientific data and the ability to translate this information to meet educational and research needs.
Demonstrated ability to address educational and research needs through delivery of cutting edge scientific/evidenced-based data.
Understanding of healthcare systems affecting patient care.
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.
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