MSD
MSD

MSD saraton, yuqumli kasalliklar, yurak-qon tomir va metabolik holatlar, shuningdek, profilaktik tibbiy yordam kabi muhim sog‘liq muammolariga qarshi dori vositalari va vaksinalarni ishlab chiqadigan global biofarmatsevtika kompaniyasidir. Amerika Qo‘shma Shtatlari, Kanada va Puerto-Rikoda Merck & Co., Inc. nomi bilan tanilgan MSD ilmiy tadqiqotlarni ishlab chiqish va tijoriy tajriba bilan birlashtirib, odamlar va hayvonlar uchun tibbiy yechimlarni taqdim etadi.

Kompaniya faoliyati Inson salomatligi, Hayvonlar salomatligi hamda Tadqiqot va ishlanmalar yo‘nalishlarini qamrab oladi. Bu ilmiy, klinik, tijoriy, operatsion va korporativ jamoalarda faoliyat yurituvchi mutaxassislar uchun imkoniyatlar yaratadi. Dunyoning turli hududlarida faoliyat olib boradigan MSDdagi martaba imkoniyatlari tadqiqot, hamkorlik, inklyuzivlik va global salomatlik sohasidagi mas’uliyatli taraqqiyotga e’tiborni aks ettiradi.

Regional Medical Scientific Director, Cardiopulmonary and Pulmonary Hypertension

Lead scientific exchange and medical affairs initiatives in pulmonary hypertension for MSD across the South Central United States. Support investigators, clinical research, external experts, and cross-functional strategy through evidence-based scientific engagement.

Tavsif

  • Lead strategic priorities involving growth, scientific innovation, and organizational change
  • Build scientific partnerships with pulmonary hypertension experts and investigators
  • Deliver balanced, factual scientific information on disease areas, company products, and company data
  • Develop peer-level relationships with national, regional, and clinical practice leaders and investigators
  • Identify scientific information needs and ensure appropriate access to medical and scientific resources
  • Lead non-product discussions covering disease states, diagnosis, epidemiology, unmet needs, and population health
  • Translate scientific exchanges into actionable insights for Research & Development and Human Health strategies
  • Share external stakeholder perspectives and feedback with Medical Affairs headquarters teams
  • Represent Research & Development at scientific meetings and congresses, contributing to debriefs, insight reviews, and post-congress reports
  • Support company-sponsored clinical trials and Investigator Study Programs as requested
  • Identify potential investigators for Phase II–IV development programs and support sponsored research
  • Provide detailed scientific support to Health Systems Teams
  • Maintain expertise in pulmonary hypertension and related therapeutic areas through conferences, workshops, and medical literature review
  • Follow company policies, applicable laws and regulations, ethical standards, field SOPs, GCP requirements, and administrative obligations
  • Help foster a workplace culture of belonging, engagement, and empowerment

Talablar

  • An M.D., Ph.D., Pharm.D., or relevant advanced practice provider qualification applicable to pulmonary hypertension
  • At least three years of experience in biotechnology, pharmaceuticals, or healthcare
  • Either three years of clinical or research experience beyond the terminal degree in cardiovascular and pulmonary therapeutic areas with demonstrated scientific excellence, or five years of Medical Scientific Liaison experience in relevant therapeutic areas with demonstrated scientific excellence
  • Strong interpersonal, communication, networking, and presentation capabilities grounded in professional integrity
  • Advanced knowledge of cardiovascular and pulmonary therapeutics and current translational science trends
  • Ability to build partnerships with scientific leaders, investigators, clinical practice leaders, academic-affiliated institutions, and treatment guideline members
  • Scientific recognition in cardiovascular and pulmonary therapeutic areas is preferred
  • Clinical practice experience and independent research or publication experience in the therapeutic area are preferred
  • Five years of prior pharmaceutical industry experience in the relevant therapeutic area or disease state is preferred
  • Prior experience in the assigned geography and established stakeholder relationships are preferred
  • Demonstrated leadership ability
  • Proficiency with Microsoft Office applications, including Word, PowerPoint, and Excel
  • Ability to organize complex datasets, plan or conduct analyses, synthesize findings, and interpret results objectively
  • Working knowledge of national and society treatment guidelines, clinical research procedures, FDA regulations, OIG, HIPAA, and other applicable ethical, legal, and regulatory requirements
  • Ability to organize priorities and perform effectively in a continuously changing environment
  • Residence within the South Central territory of Tennessee, Alabama, Mississippi, Louisiana, or Kentucky
  • Valid driving license
  • Willingness to travel 50%
  • Visa sponsorship is not available

Imtiyozlar

  • Annual bonus
  • Long-term incentive where applicable
  • Medical, dental, and vision coverage for employees and their families
  • Additional insurance coverage for employees and their families
  • Retirement benefits including a 401(k) plan
  • Paid holidays
  • Vacation leave
  • Compassionate and sick leave
  • Remote work arrangement