Regional Medical Scientific Director – Myeloid

Job not on LinkedIn

🔥 25 minutes ago

🏈 Alabama, Florida, +3 more states – Remote

🏈 Alabama – Remote 🐊 Florida – Remote ⚜️ Louisiana – Remote 🎸 Mississippi – Remote 🔔 Pennsylvania – Remote

💵 $210.4k - $331.1k / year

⏰ Full Time

🔴 Lead

👔 Director

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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MSD

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1891

🏥 Healthcare

📦 Logistics

🧬 Biotechnology

Healthcare • Logistics • Biotechnology

MSD is a leading biopharmaceutical company known as Merck & Co. , Inc. in the United States, Canada, and Puerto Rico, and as MSD globally. The company focuses on scientific innovation to deliver medicines and vaccines for various health challenges, including oncology, vaccines, infectious diseases, and cardio-metabolic diseases. MSD operates multiple divisions, including Human Health, Animal Health, and Research & Development. With approximately 75,000 employees worldwide and a significant investment in research and development, MSD is committed to improving global health through its scientific advancements. Additionally, the company places a strong emphasis on diversity, inclusion, and corporate responsibility. MSD’s operations extend worldwide, offering opportunities in numerous regions and promoting diversity and innovation in all aspects of its business.

📋 Description

• Engage in bidirectional scientific and medical information exchange with Scientific Leaders • Provide balanced, factual, scientific information about non-product areas and respond to scientific questions, including questions about Company products • Develop professional relationships with national and regional Scientific Leaders • Conduct peer-to-peer scientific discussions and maintain a reliable medical contact presence • Address scientific questions and direct out-of-scope inquiries to appropriate company resources • Maintain current knowledge of the scientific and clinical environment in the relevant therapeutic area • Initiate discussions with Scientific Leaders and potential investigators regarding scientific/data exchange, research strategies, study concepts, scientific merit, and qualifications • Enhance understanding of the scientific foundations and goals of investigator-sponsored research • Identify barriers to patient enrollment and retention • Recommend study sites and identify potential investigators for phase II-IV clinical development programs • Conduct Site Initiation Visits and support patient enrollment and retention efforts • Collaborate with Global Clinical Trial Operations on protocol leadership responsibilities • Address investigator questions and provide information about Company-sponsored clinical studies • Engage in scientific congresses and medical meetings and facilitate scientific and data exchange • Gather feedback and insights about medical or scientific needs, priorities, and concerns of Scientific Leaders and/or patients • Serve as a role model for field medical team members through onboarding and sharing therapeutic expertise • Contribute to an environment of belonging and empowerment

🎯 Requirements

• PhD, PharmD, DNP, DO, or MD • Minimum of 3 years of relevant therapeutic area experience beyond that obtained in the terminal degree program • Ability to conduct doctoral-level discussions with key external stakeholders • Dedication to scientific excellence with a strong focus on scientific education and dialogue • Excellent stakeholder management, communication, and networking skills • Thorough comprehension of FDA, OIG, HIPAA, and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers • Ability to organize, prioritize, and work effectively in a constantly changing environment • Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Teams, OneNote) • Familiarity with virtual meeting platforms • Desire to contribute to an environment of belonging and empowerment • Consistent adherence to field and corporate policies and Global Medical Scientific Affairs strategy, including field SOPs, GCP guidelines, and administrative/operational responsibilities • Candidates must reside within the territory covering FL, GA, AL, AR, LA, and MS • Ability to travel up to 50% within the territory • Malignant Hematology, Medical Affairs, Medical Knowledge, Oncology, Pharmaceutical Medical Affairs, Professional Networking, Scientific Communications, Scientific Research, and Stakeholder Engagement • External Collaboration, Hematology and Oncology, Pharmaceutical Industry, Science Outreach, and Stakeholder Management

🏖️ Benefits

• Annual bonus • Long-term incentive, if applicable • Medical, dental, and vision healthcare • Other insurance benefits for employee and family • Retirement benefits, including 401(k) • Paid holidays • Vacation • Compassionate days • Sick days • Remote work arrangement • Accommodation during the application or hiring process, where needed

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