Regional Medical Scientific Director – Cardiopulmonary, Pulmonary Hypertension

Job not on LinkedIn

🔥 11 minutes ago

🏈 Alabama, Kentucky, +3 more states – Remote

🏈 Alabama – Remote 🐎 Kentucky – Remote ⚜️ Louisiana – Remote 🎸 Mississippi – Remote 🎸 Tennessee – 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 growth, scientific innovation, and organizational adaptation • 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 • Develop and manage peer-level relationships with national, regional, and clinical practice scientific leaders and investigators • Identify and address scientific needs and ensure access to medical and scientific information • Conduct proactive non-product discussions on disease states, diagnosis, epidemiology, unmet medical need, and population health • Facilitate scientific information exchange and provide actionable insights to inform 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, insight discussions, and post-congress reports • Support company-sponsored trials and Investigator Study Programs as requested • Identify potential investigators for phase II-IV clinical development programs and support 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, applicable laws, regulations, ethical standards, field SOPs, GCP guidelines, and administrative responsibilities • Contribute to an environment of belonging, engagement, and empowerment

🎯 Requirements

• M.D., Ph.D., Pharm.D. or APP relevant to the Pulmonary Hypertension area • Three years in the biotech/pharmaceutical or healthcare environment • Three years clinical and/or research experience beyond the terminal degree program in Cardiovascular & Pulmonary therapeutic areas and demonstrated scientific excellence, or five years of Medical Scientific Liaison experience in relevant therapeutic areas and demonstrated scientific excellence • Principled interpersonal, communication, networking, and presentation skills • Deep therapeutic competency and knowledge of current trends in Cardiovascular & Pulmonary/translational science • Ability to network and partner with scientific leaders, investigators, clinical practice leaders, academic-affiliated institutions, and treatment guideline members • Preferred recognition for scientific excellence in Cardiovascular & Pulmonary therapeutic areas • Preferred clinical therapeutic area practice and independent research/publication experience • Preferred five years of prior pharmaceutical industry experience in the relevant therapeutic area/disease state • Preferred prior experience within the given geography and established stakeholder relationships • Demonstrable effective leadership skills • Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel) • Ability to consolidate and understand complex data sets, plan and/or execute data analyses, summarize or synthesize data, and objectively interpret results • Knowledge of national and society treatment guidelines, clinical research processes, FDA regulations, OIG, HIPAA, and other relevant ethical guidelines, laws, and regulations • Ability to organize, prioritize, and work effectively in a constantly changing environment • Must reside within the defined South Central territory: Tennessee, Alabama, Mississippi, Louisiana, or Kentucky • Valid driving license required • 50% travel • No visa sponsorship

🏖️ Benefits

• Annual bonus • Long-term incentive, if applicable • Medical, dental, and vision healthcare benefits for employee and family • Other insurance benefits for employee and family • Retirement benefits, including 401(k) • Paid holidays • Vacation • Compassionate and sick days • Remote work arrangement