MSL Dermatology Dupilumab (CO, AZ, UT, WY)

Sanofi•Denver, CO

7d•Remote

About The Position

As a Medical Science Liaison, Dermatology Dupilumab within Sanofi's R&D team, you will serve as a trusted scientific partner in the field for external experts and decision-makers, engaging in mutual scientific exchanges to accelerate data dissemination. Sanofi's Medical Field-based teams enhance the understanding of the scientific and medical value of our products in the therapeutic area and gather new insights by bringing cutting-edge scientific exchange today that accelerates medical innovation tomorrow. In this role, you will manage a base of 55 stakeholders, developing and maintaining a stakeholder engagement tracking database. You will plan day-to-day interactions, including discussion points in accordance with Medical Affairs strategy, establishing a frequency of interactions per stakeholder per year to ensure that objectives are met. This position has accountability at the US level with reporting primarily to Medical Affairs. You will execute on a defined KOL territory strategy that is targeted to address diverse stakeholder needs (payers, patients, KOLs, HCPs, etc.) and is aligned with company objectives. Additionally, you will develop relevant territory engagement plans in line with the medical strategy, support the team's medical plan execution, and use approved scientific data during KOL interactions to advance the understanding of the therapeutic area. Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you’ll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs.

Requirements

1+ year as a Medical Science Liaison (MSL) or in clinical practice within Dermatology OR 3+ years as an MSL in an adjacent therapeutic area with a strong Immunology background.
Dermatology MSL experience strongly preferred
Clinical dermatology provider experience is a plus
Advanced degree required in a technical, scientific, or medical field (MD, PhD, PharmD, or equivalent)
Previous pharmaceutical or biotech industry experience preferred
Comprehensive understanding of medical practice, clinical decision-making, and healthcare systems as they relate to patient care
Knowledge of research study design, execution, and interpretation
Ability to critically interpret and evaluate key scientific data and clinical evidence
Skill in translating complex scientific information to address educational and research needs of healthcare professionals
Proven ability to deliver cutting-edge, evidence-based scientific presentations
Exceptional verbal and written communication skills
Outstanding presentation and platform skills
Demonstrated success working collaboratively on cross-functional, multi-disciplinary teams
Strong project management capabilities with ability to manage multiple priorities simultaneously

Nice To Haves

Actively listens to others and is adept at confidently stating expert opinion while respecting the positions of others - can exert diplomacy while standing firm on a position.
Utilizes effective, professional communications to cultivate strong working relationships with internal and external colleagues, flexible in own approach to people and situations.
Skilfully plans, prioritizes, and executes multiple responsibilities and projects.
Demonstrates effective leadership skills (by example and through accomplishments), steps forward to handle challenges within scope of authority.
Deep understanding and knowledge of local regulations and codes of practice for pharmaceutical industry, in particular as they apply to the non-promotional activities of this role .
Demonstrates scientific expertise - stays abreast of data, treatment trends, and new information in the profession and ability to articulate therapeutic knowledge and translate expert feedback into appropriate insights.
Knowledge of relevant healthcare systems, the evolving medical landscape, regulatory and payer environment, public health and industry trends.
Proficiency in digital tools.

Responsibilities

Serve as a trusted scientific partner to Key Opinion Leaders and external experts by conducting timely, high-quality scientific exchanges that enhance understanding of the medical and scientific value of Sanofi's products.
Gather, record, and critically evaluate data from stakeholder interactions and published studies to develop key insights that deepen understanding of patient, HCP, payer, and regulator needs, contributing to Sanofi's scientific messages, plans, and strategy.
Maintain up-to-date knowledge of therapeutic areas, disease management protocols, healthcare policies, and competitive landscape to articulate the medical value of products and support evidence-based discussions with external stakeholders.
Leverage the Scientific Engagement Model to plan territory and individual stakeholder strategies, prioritize KOLs and HCPs, and establish Sanofi's medical presence at scientific congresses, symposia, and advisory boards.
Maintain effective communication with Medical Affairs, Medical Information, and Commercial Operations colleagues while ensuring full compliance with company, industry, legal, and regulatory requirements and excellence in governance processes.
Support evidence generation activities including protocol development, pharmacovigilance, effectiveness studies, clinical trial site identification, and Investigator Sponsored Study (ISS) submissions through approved processes.
Respond to unsolicited requests for medical information, organize educational meetings, support speaker training, and contribute to the creation of materials for internal and external stakeholders following Sanofi and regulatory policies.