Regional Medical Scientific Director – Uro-Oncology

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

📋 Description

• Foster professional relationships and engage with Urology Scientific Leaders on both national and regional levels.

• Facilitate peer-to-peer scientific discussions while maintaining dependable scientific connections.

• Address scientific inquiries and appropriately direct out-of-scope questions to relevant company resources.

• Review education and training initiatives directed by headquarters.

• Act as a liaison between the scientific community and the company for sponsored clinical trials and investigator-sponsored research.

• Identify challenges related to patient enrollment and retention, recommending suitable study sites and investigators.

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

• Evaluate investigator studies in relation to research strategies, study concepts, scientific merit, and qualifications.

• Prepare for and engage in scientific and medical congresses.

• Facilitate the exchange of scientific data involving both company and competitor information.

• Collect valuable scientific insights and support congress exhibit booths as needed.

• Gather input regarding medical and scientific needs, priorities, and concerns.

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

• Function independently without sales targets or accountability for prescribing or product sales.

⛳️ Requirements

• PhD, PharmD, DNP, or MD required.

• Clinical (patient care) or research experience in assigned therapeutic areas, beyond what was acquired during the terminal degree program.

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

• At least 3 years of experience in therapeutic areas related to Oncology or Urology.

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

• Strong emphasis on scientific education and dialogue.

• Business acumen and market knowledge.

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

• Comprehensive understanding of FDA, OIG, HIPAA, and other ethical guidelines, laws, and regulations pertinent to the pharmaceutical industry and its clients.

• Capability to organize, prioritize, and work efficiently in a dynamic environment.

• Proficient knowledge of Microsoft Office Suite (Word, Excel, PowerPoint, Outlook, MS Teams, MS Copilot).

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

• Willingness to travel overnight up to 50% of the time.

• Must reside in the TN, AL, NC, SC, GA, or FL territory.

• A valid driving license is required.

• Visa sponsorship is not available.

🏝️ Benefits

• Eligibility for an annual bonus.

• Eligibility for long-term incentives, if applicable.

• Comprehensive medical, dental, and vision healthcare.

• Additional insurance benefits for employees and their families.

• Retirement benefits including a 401(k) plan.

• Paid holidays.

• Vacation time.

• Compassionate leave.

• Sick leave.

• Flexibility for remote work arrangements.