Regional Medical Scientific Director – Uro-Oncology

This is a fully remote position, open to applicants in Illinois, +3 more states.

📋 Description

• Engage in scientific dialogue with national and regional Urology Scientific Leaders.

• Provide unbiased, factual, and scientific information regarding non-product areas of interest as well as company products.

• Address scientific inquiries and redirect out-of-scope questions to the appropriate resources within the company.

• Stay updated through education and training directed by headquarters.

• Develop professional relationships and facilitate peer-to-peer scientific discussions with Urology Scientific Leaders.

• Act as a liaison between the scientific community and the company concerning Company-Sponsored Trials and Investigator-Sponsored Program research.

• Identify challenges related to patient enrollment and retention, suggest study sites, and pinpoint potential investigators for Phase II-IV programs.

• Respond to investigator inquiries regarding company-sponsored clinical studies.

• Initiate discussions on scientific data exchange related to research strategies, study concepts, scientific merit, and qualifications.

• Prepare for and engage in scientific congresses, share scientific and medical data, collect insights, and manage exhibit booths as required.

• Collect feedback and information on medical or scientific needs, priorities, and concerns.

• Serve as a mentor for field medical team members, including onboarding and therapeutic training.

• Operate without sales goals or responsibilities related to prescribing or sales.

⛳️ Requirements

• PhD, PharmD, DNP, or MD.

• Clinical patient care or research experience in relevant therapeutic areas beyond the terminal degree program.

• Experience as a field-based medical science liaison (MSL).

• At least 3 years of experience in the therapeutic area of Oncology or Urology.

• Ability to engage in doctoral-level discussions with key external stakeholders.

• Knowledge of business and market dynamics.

• Strong skills in stakeholder management, communication, and networking.

• In-depth understanding of FDA, OIG, HIPAA, and other pertinent pharmaceutical industry ethical guidelines, laws, and regulations.

• Capacity to organize, prioritize, and work efficiently in a fast-paced environment.

• Proficient in Microsoft Office Suite, including Word, Excel, PowerPoint, Outlook, MS Teams, and MS Copilot.

• Compliance with field and corporate policies, GMSA strategy, field SOPs, GCP guidelines, and administrative/operational responsibilities.

• Willingness to travel up to 50% overnight.

• Must reside within the territory of WI, IL, IN, MI, or OH.

• Valid driver’s license.

🏝️ Benefits

• Annual bonus.

• Long-term incentive, if applicable.

• Medical, dental, and vision healthcare.

• Additional insurance benefits for employees and their families.

• Retirement benefits, including 401(k).

• Paid holidays.

• Vacation.

• Compassionate days.

• Sick days.

• Remote work arrangement.