Medical Science Liaison- Pulmonary- Chicago (IL/WI/IN)

Sanofi•Cambridge, MA

21h•Remote

About The Position

As Medical Science Liaison, Pulmonary - Chicago (IL/WI/IN) within our 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. Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.

Requirements

Advanced degree (MD, PhD, Pharm D,) preferred, or other Relevant Life Sciences Degree (RN/MS) with Healthcare Specialty required
More than 2 years of experience in medical affairs
Minimum of 2 years MSL Experience preferred.
Experience in local, regional, and/or global medical function roles
Demonstrable high level of strategic thinking related to Stakeholder mapping
Proven abilities in Scientific/Medical engagement, stakeholder plan development and the ability to gather and translate scientific data into appropriate insights and clinical discussion points which support the medical strategy
Demonstrates effective leadership skills (by example and through accomplishments), steps forward to handle challenges within scope of authority and its able to transmit this knowledge to other members of the team
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 .
Ability to readily acquire scientific and clinical understanding of the therapeutic area, medical practices, clinical cases, and disease management best practices
Strong technical expertise in the areas of product knowledge, product development, and clinical development.
High degree of knowledge of relevant healthcare systems, the evolving medical landscape, regulatory and payer environment, public health and industry trends
Proficiency in planning for and engaging with the HCP environment using digital tools
Working knowledge of English (as a second language)

Responsibilities

Be the trusted scientific partner to key external experts by conducting timely, appropriate and frequent scientific exchanges to enhance the understanding of the scientific and medical value of our products
Develop robust stakeholder engagement plans to gather data, develop and share medical insights that contribute to enhancement of Sanofi’s key medical messages, plans and future research
Exhibit a high degree of scientific and clinical knowledge in the therapeutic field to help identify and critically assess research opportunities and to play a supportive role in the execution of evidence generation plans to enhance the value of our products in a real-world setting
Effortlessly and consistently identify insights that deepen our understanding of the needs of patients, consumers, regulators, payers, and healthcare providers and proactively identifies unmet needs
Maintain effective and appropriate communication and collaboration among internal stakeholders (Medical Affairs colleagues, Medical Information and Commercial Operations) while maintaining full compliance with relevant company, industry, legal and regulatory requirements
Demonstrate operational understanding and risk management by ensuring excellence in execution within the boundaries of all governance processes
Engages external stakeholders on medical and scientific information exchange for the therapeutic area during an one-on-one interactions and group settings, exhibiting excellent scientific and clinical knowledge
Applies broad and deep knowledge of relevant diseases and disease management protocols, healthcare environment and competitors to articulate the medical and scientific value of our products
Establishes robust, long-term peer relationships with thought leaders and other stakeholder partners
Leads high-level stakeholder engagement discussions on medical, clinical, epidemiologic, and scientific topics with Healthcare Practitioners to advance their understanding of the disease by sharing information and answering questions based on approved material within corporate, industry and regulatory guidelines
Engages with appropriate stakeholders to understand the impact of healthcare policies and guidelines as they relate to clinical practices at a local, state, regional, federal, or national level.
Uses systems to strategically maps, identify, profile, and prioritizes stakeholder in line with the therapeutic area (TA) Medical plan and creates a collaboration pathway to address the HCPs therapeutic goals
Independently utilizes the Scientific Engagement Model to plan and create territory and individual stakeholder (KOL, payers, HCP etc..) medical strategy and engagement plans consistent with country, regional and global medical function priorities and routinely evaluates the effectiveness of plan
Effectively utilizes the Scientific Engagement Model in leading the planning and strategically organizing local/regional scientific congresses, symposia attendance, gathers observations and insights and ensures follow up of outstanding action items
Organizes educational meetings or local scientific advisory boards
Provides effective clinical presentations to internal and external audiences and tailors presentations to meet specific needs of the audience.
Support speakers training to ensure continued scientific support in the field
Responds to unsolicited request for medical information associated with supported products and disease state areas.
Gathers data and generates insights from stakeholder interactions and provides feedback to the organization
Independently recognizes and elaborates on potential issues or topics of interest to the company, including but not limited to competitor activity, during stakeholder interactions
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 to inform and enable the medical strategy
Records/reports insights and information appropriately, using available mechanisms and tools
Strategically evaluates published studies and discerns, from the information and opinions gained from stakeholder interactions, key insights that deepen our understanding of the therapeutic area unmet needs and enhancement of Sanofi’s scientific messages, strategic plans, systems, and product development.
Proactively uses available tools and databases (MedMeme/Doctor Evidence/MedLine/Trial Trove etc) to search and assess emerging evidence in disease area to enable and enhance scientific discussions with key stakeholders
Proactively identifies unmet needs that could be addressed through novel indications, combinations or formulations, etc. and communicates these to internal stakeholders appropriately
Collaborates routinely and effectively with internal stakeholders
Partners with internal stakeholders , Commercial Operations, Business Development, Regulatory, etc. to facilitate internal distribution of key external insights diligence reviews, medical and safety evaluation, product positioning, lifecycle evidence planning, and compliance needs when requested
Distributes and trains on relevant scientific and medical information to internal stakeholders
Contributes to the creation of material for internal and external stakeholders following internal Sanofi policies, and Federal and National Policies as applicable
Provides training to, or advises internal stakeholders and other MSL Team members, acting as a role model for MSL Behaviours
Takes scientific data and translates it into clinical discussion points that support business objectives and medical brand strategy
Supports evidence-generation activities by aiding in data acquisition and identifying opportunities for further data collection clinical or investigator-led
Maintains a high level of understanding on disease epidemiology and treatment pathways and provides support, including protocol development, when needed, on various types of studies: long-term surveillance, compliance, pharmacovigilance, and effectiveness studies
Maintains awareness of clinical investigator activities throughout territory and offers suggestions on appropriate clinical trials sites when appropriate
Identifies data collection opportunities and recognizes opportunities to gather Real World Evidence within the territory and informs internal stakeholders using appropriate channels.
Responds to unsolicited requests regarding interest in investigator sponsored studies (ISS), and supports ISS submissions through appropriate internal processes.