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

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…