Medical Science Liaison - TX, OK, LA, AR, MS Science - Providence, RI at Geebo

Medical Science Liaison - TX, OK, LA, AR, MS

The Medical Science Liaison (MSL) will be responsible for:
Providing non-promotional scientific, educational, and research support for the Rare Disease 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).
The MSL will be responsible for developing and maintaining relationships with key experts and building a well-informed advocacy base for Sanofi's Rare Disease 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 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.
This is a field based position, with a territory that includes TX, OK, LA, AR and MS.
The ideal candidate will live near Dallas, TX, near a major airport within the territory, or be willing to relocate at their own expense.
Job Responsibilities Maintains business and clinical knowledge of rare disease landscape including current treatment strategies, current and pending competitors, and new therapeutic developments.
Increases Sanofi's visibility among leaders in the therapeutic field of Rare Disease (PAGE).
Identifies, establishes and maintains collaborative relationships with key 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 clinical team and CRA's to coordinate and optimize educational and research support for sites/investigators participating in Sanofi'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 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 needs of Key Opinion leaders (KOLs).
Maintains clinical expertise through comprehensive education including attendance at 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 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.
Education:
PharmD, PhD,CGC,MDor other advanced degree required 2 years related pharma/biotech experience
Experience:
Knowledge and experience in Rare Disease, specifically rare genetic conditions, strongly preferred.
1
years of MSL or equivalent experience strongly 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 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.
Ability to understand and speak Spanish is helpful but not required.
#GD-SG#LI-GZAt 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.
Recommended Skills Administration Biotechnology Clinical Trials Clinical Works Consulting Decision Making Estimated Salary: $20 to $28 per hour based on qualifications.

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