Regional Medical Scientific Director – Cardiopulmonary, Pulmonary Hypertension

🔥 6 minutes ago

🌾 Iowa, Kansas, +2 more states – Remote

🌾 Iowa – Remote 🌪️ Kansas – Remote 🌾 Nebraska – Remote 🏰 Missouri – Remote

💵 $190.8k - $300.3k / 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

• Drive strategic operating priorities related to scientific innovation, resource prioritization, organizational adaptation, and diverse talent • Engage in scientific exchange and research support with external scientific leaders and investigators in Pulmonary Hypertension • Provide balanced, factual scientific information about non-product areas, company products, and company data • Facilitate and develop peer-level relationships with scientific leaders and investigators • Identify and address scientific needs and ensure access to medical and scientific information • Conduct peer-level scientific discussions and maintain a reliable Medical Affairs contact presence • Lead proactive non-product discussions on disease states, diagnosis, epidemiology, unmet medical need, and population health • Integrate scientific knowledge into actionable insights for Research & Development and Human Health strategies • Communicate external stakeholder opinions, insights, and feedback to Medical Affairs headquarters teams • Represent Research & Development at scientific meetings and congresses and contribute to debriefs and post-congress reports • Support company-sponsored trials and Investigator Study Programs • Identify potential investigators for Phase II-IV clinical development programs • Provide scientific support for sponsored trials • Provide in-depth scientific support to Health Systems Teams • Maintain disease and therapeutic-area expertise through conferences, workshops, and journal review • Comply with company policies, laws, regulations, ethical standards, field SOPs, GCP guidelines, and operational responsibilities • Contribute to an inclusive, equitable, engaged, and empowering environment

🎯 Requirements

• M.D., Ph.D., Pharm.D. or relevant APP credential required • Three years in the biotech/pharmaceutical or healthcare environment • Three years of clinical and/or research experience beyond the terminal degree program in Cardiovascular & Pulmonary therapeutic areas, with demonstrated scientific excellence, or five years of relevant Medical Scientific Liaison (MSL) experience with demonstrated scientific excellence • Principled interpersonal, communication, networking, and presentation skills • Deep therapeutic competency and current knowledge of Cardiovascular & Pulmonary/translational science trends • Ability to network and partner with scientific leaders, investigators, clinical practice leaders, academic-affiliated institutions, and treatment guideline members • Recognition for scientific excellence in Cardiovascular & Pulmonary therapeutic areas preferred • Clinical therapeutic-area practice and independent research/publication experience highly desirable • Five years of prior pharmaceutical industry experience preferred • Prior experience within the geography and established therapeutic-area stakeholder relationships preferred • Effective leadership skills preferred • Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel) preferred • Ability to consolidate and understand complex data sets, execute data analyses, summarize/synthesize data, and objectively interpret results preferred • Knowledge of national and society treatment guidelines, clinical research processes, FDA regulations, OIG, HIPAA, and relevant ethical guidelines, laws, and regulations preferred • Ability to organize, prioritize, and work effectively in a changing environment preferred • Up to 50% travel, including overnight • Must reside within the defined Central Plains territory: Missouri, Kansas, Arkansas, Nebraska, or Iowa • Valid driving license required • No visa sponsorship

🏖️ 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 • No relocation