Regional Medical Scientific Director (Medical Science Liaison) - Cardiovascular & Metabolism - Il & IN (Remote)

Job Description

Regional Medical Scientific Director – Cardiovascular & Metabolism

The Cardiovascular & Metabolism Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). This MSL-type role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work of an RMSD is aligned to: Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights.

Cardiovascular & Metabolism RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies. The RMSD serves as a role model for other field medical team members in ways that include on-boarding and/or sharing of therapeutic expertise.

Location details:  This role covers Illinois and Indiana.  Candidates must reside within the territory with expected travel up to 50% within the territory.

Responsibilities and Primary Activities

Scientific Exchange:

• Develops professional relationships and engages with national and regional SLs to ensure access to company-approved medical and scientific information on areas of therapeutic interest and Company products

• Conducts peer-to-peer scientific discussions and maintains a reliable presence with those SLs to ensure they have a medical contact within the company

• Addresses scientific questions and directs SL inquiries on issues outside of RMSD scope (e.g., grants) to appropriate company resources consistent with applicable policies

• Maintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI) for the RMSD’s specific therapeutic area.

Research:

• Upon request from Global Center for Scientific Affairs (GCSA),

• Initiates discussions with SLs and/or potential investigators that include scientific/data exchange within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial

• Enhances the comprehension of the scientific foundations and goals of investigator-sponsored research

• Identifies barriers to patient enrollment and retention efforts to achieve study milestones

• Upon request from Global Clinical Trial Operations (GCTO),

• Recommends study sites and identifies potential investigators to participate in phase II-IV clinical development programs, conducts Site Initiation Visits (SIVs), and detects barriers to patient enrollment and retention efforts to achieve study milestones.

• Protocol lead responsibilities in collaboration with GCTO

• Addresses questions from investigators and provides information regarding participation in Company-sponsored clinical studies

Scientific Congress Support:

• Engages in scientific congresses and medical meetings, facilitates scientific and data exchange for both Company and competitor data.

 Scientific Insights:

• Gathers feedback, data, or information during routine activities that can help the company better comprehend medical or scientific needs, priorities, or concerns of SLs and/or patients

Inclusive Mindset and Behavior:

• Demonstrates eagerness to contribute to an environment of belonging, inclusion, equity, and empowerment

• Leads by example and serves as a role model for creating, leading, and retaining a diverse and inclusive workforce

 Required Qualifications, Skills, & Experience

Minimum:

• PhD, PharmD, DNP, DO, or MD

• Proven competence and a minimum of 3 years of relevant therapeutic area experience beyond that obtained in the terminal degree program, e.g.,  Atherosclerosis

• Ability to conduct doctoral-level discussions with key external stakeholders

• Dedication to scientific excellence with a strong focus on scientific education and dialogue

• Excellent stakeholder management, communication, and networking skills

• A thorough comprehension of FDA, OIG, HIPAA, and other ethical guidelines, laws, and regulations relevant to t