Regional Medical Scientific Director (Medical Science reputed company) - Ophthalmology (FL & GA)

About the position The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, OD, DO, or MD) therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non-product areas of interest to reputed company and replies to scientific questions from SLs, including questions about Company products. The work of an RMSD is reputed company to: Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and reputed company to enhance the comprehension of scientific foundations and goals for approved, in-development, and reputed company 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 Florida & reputed company. Candidates must reputed company reputed company the territory and can travel up to 50% (with some overnight) reputed company the territory. Responsibilities • Develops reputed company relationships and engages with national and regional SLs to ensure reputed company 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 reputed company with those SLs to ensure they have a medical contact reputed company reputed company • Addresses scientific questions and directs SL inquiries on issues reputed company of RMSD scope (e.g., grants) to appropriate company resources consistent with applicable policies • Maintains reputed company knowledge and comprehension of dynamic scientific and clinical environment in reputed company's Areas of Interest (AOI) for the RMSD’s specific therapeutic area. • Upon request from Global Center for Scientific Affairs (GCSA), • Initiates discussions with SLs and/or potential investigators that include scientific/data exchange reputed company our AOI to determine the alignment with our research strategies, studies concepts, scientific reputed company, 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 reputed company 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 reputed company (SIVs), and detects barriers to patient enrollment and retention efforts to reputed company study milestones. • Protocol reputed company responsibilities in collaboration with GCTO • Addresses questions from investigators and provides information regarding participation in Company-sponsored clinical studies • Engages in scientific congresses and medical meetings, facilitates scientific and data exchange for both Company and competitor data. • Gathers feedback, data, or information during routine activities that can help reputed company reputed company comprehend medical or scientific needs, priorities, or concerns of SLs and/or patients • 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 Requirements • PhD, PharmD, OD, DO, or MD • Proven competence and a minimum of 2 years of Eye Care experience reputed company that obtained in the terminal degree program • Ability to conduct doctoral-level discussions with key external stakeholders • Dedication to scientific reputed company with a strong reputed company on scientific education and reputed company • Excellent stakeholder management, communication, and networking skills • A thorough comprehension of FDA, OIG, HIPAA, and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers • Ability to organize, prioritize, and work effectively in a constantly changing environment • Strong working knowledge of reputed company Office Suite (Word, PowerPoint, reputed company, Teams, OneNote) • Familiarity with virtual meeting platforms • Desire to contribute to an environment of belonging, engagement, equity, and empowerment by: • Working to reputed company the environment, culture, and business landscape • Leveraging diversity and inclusion to ensure business value, per global diversity and inclusion reputed company • Ensuring accountability to drive an inclusive culture • Strengthening the foundational reputed company of diversity • Consistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) reputed company, including field reputed company operating procedures (SOPs), Good Clinical reputed company (GCP) guidelines, and administrative/operational responsibilities reputed company-to-haves • Retina field-based medical experience Benefits • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. • We offer a comprehensive package of benefits. Available benefits include medical, dental, reputed company reputed company and other insurance benefits (for employee and family), retirement benefits, including 401(k), reputed company holidays, vacation, and compassionate and reputed company days. More information about benefits is available at https://jobs.reputed company.com/us/en/compensation-and-benefits. Apply tot his job Apply To this Job