Regional Medical Scientific Director; RMSD; Uro-Oncology; Lakes

The-Regional-Medical Scientific Director (RMSD) is a credentialed (i.e.,-PhD,-PharmD,-DNP, MD) therapeutic and disease expert who engages in scientific exchange with-leaders-in the external medical and scientific community. RMSDs provide to Scientific-Leaders-(SLs) balanced, factual, scientific information about non-product areas of interest to the company.

-RMSDs reply to scientific questions from SLs, including questions about company products. The work of an RMSD is aligned to-the core-pillars:

-Scientific Exchange, Clinical Research, Scientific Congress Support, and Scientific Insights.

• Develop professional relationships and engage with national and regional-Urology SLs-to ensure access to medical and scientific information on areas of therapeutic interest and company products.
• Conduct peer-to-peer scientific discussions and maintain a reliable presence with-those-SLs-to ensure they have a medical contact within the company.
• Address scientific questions and direct-SL-inquiries on issues outside of-RMSD-scope (e.g. grants) to appropriate company resources consistent with applicable policies.
• Review HQ-directed education and training to maintain current knowledge and comprehension of dynamic scientific and clinical environment in the company's areas of interest.

Scientific exchange does not include promotional claims about any drug, vaccine or biologic product.

-RMSDs have no sales objectives or accountability for prescribing or sales of any company product and are required-to avoid any situations that could create the appearance that they have such-responsibilities. A-RMSD-may not comment on or make suggestions with respect to the diagnosis, treatment, or circumstances of a specific patient.

• Liaison between the scientific community and company to enhance the comprehension of scientific foundations and goals for approved, in development and active Company-Sponsored Trials and/or our Company's Investigator-Sponsored Program-(MISP) research studies.

• Identify barriers to patient enrollment and retention efforts to achieve study milestones, recommend study sites, and identify potential investigators to participate in phase II-IV clinical development programs.
• Address questions from investigators and provide information regarding participation in our Company-sponsored clinical studies.

• Enhance the comprehension of the scientific foundations and goals of our company Investigator Studies Program (MISP)-research.
• Identify barriers to patient enrollment and retention efforts to achieve study milestones.
• Initiate discussions with SLs and/or potential investigators that include scientific/data exchange within our Areas of Interest (AOIs) to determine the alignment with our research strategies, study concepts, scientific merit, and qualifications for a specific compound or trial.

• Engage-in-scientific and medical meetings through pre-congress preparation, facilitate scientific and data exchange for both our Company and competitor data, collect meaningful insights, and staff congress exhibit booth as applicable.

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

• Serve as a role model for other field medical team members, including on-boarding and/or therapeutic training.

• PhD,-PharmD,-DNP, or MD.

• Clinical (patient care) or research experience-in assigned therapeutic area(s) beyond that obtained in the terminal degree-program.
• Field-based medical-science liaison (MSL) experience.
• A minimum of-3 years of-therapeutic area-experience-in Oncology or Urology.
• Capable of conducting doctoral level discussions with key external stakeholders.
• Dedication to scientific excellence with a strong focus on scientific education and dialogue.
• Business and market knowledge.
• Excellent stakeholder management, communication, and networking skills.
• Must-possess a thorough comprehension of-FDA, OIG, HIPAA-and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers.
• Must-be able to organize, prioritize, and work effectively in a constantly changing environment.
• Strong working knowledge of…