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

Remote / Online - Candidates ideally in
Denver, Denver County, Colorado, 80285, USA
Listing for: MSD
Remote/Work from Home position
Listed on 2026-10-03
Job specializations:
  • Healthcare
    Medical Science Liaison, Clinical Research
Salary/Wage Range or Industry Benchmark: 159000 - 251000 USD Yearly USD 159000.00 251000.00 YEAR
Job Description & How to Apply Below
Position: Regional Medical Scientific Director (RMSD) - Uro-Oncology (Southeast)
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Job Description

Scientific Exchange
  • 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.

Clinical Research
  • 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.

Upon request from Global Clinical Trial Operations (GCTO):

  • 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.

Upon request from Global Center for Scientific Affairs (GCSA):

  • 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.
Scientific Congresses
  • 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.
Scientific Insights

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.

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

PhD, PharmD, DNP, or MD.

Required Experience and Skills
  • 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 Microsoft Office Suite (Word, Excel, PowerPoint, Outlook, MS Teams, MS Copilot).
  • Consistently adhere to field and corporate policies, and Global Medical Scientific Affairs (GMSA) strategy, including field SOPs, GCP guidelines, and administrative/operational responsibilities.
  • Requires up to 50% overnight travel.
Preferred Experience and Skills
  • MSL field experience in the Urology practice setting.
  • Therapeutic experience in Genitourinary (GU) cancers (bladder, renal, prostate).
  • Established relationships with Urology SLs within geographic region.
Location
  • This is a remote position that serves the…
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