Program Development & Training Director

🕒 vor 20 Tagen

🏖️ New Jersey – Remote

🏖️ New Jersey – Remote

💵 $187.100 - $327.500 / Jahr

⏰ Vollzeit

🔴 Experte

👔 Direktor

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Novo Nordisk

WebsiteLinkedInAlle Stellen

10.000+ Mitarbeiter

Gegründet 1923

⚕️ Krankenversicherung

💊 Pharmazie

🧬 Biotechnologie

Healthcare Insurance • Pharmaceuticals • Biotechnology

Novo Nordisk ist ein globales Gesundheitsunternehmen, das seit über 25 Jahren an vorderster Front der Forschung bei Adipositas und Diabetes steht. Ihre Mission ist es, das Leben von Menschen, die an Adipositas und Diabetes leiden, durch innovative Behandlungen und nachhaltige Praktiken zu verbessern. Mit einem starken Engagement für die Patientensicherheit bekämpft Novo Nordisk aktiv gefälschte Medikamente und strebt danach, die Integrität ihrer Produkte zu verbessern. Sie bieten eine Reihe lebensrettender Medikamente an und setzen sich dafür ein, Veränderungen in der Gesundheitslandschaft voranzutreiben, um sicherzustellen, dass Kinder und Erwachsene gleichermaßen Zugang zu essentieller medizinischer Versorgung haben.

Beschreibung

• Responsible for development and execution of the content and training plan ensuring Medical Affairs has scientific resources and knowledge needed to help facilitate customer engagement. • Work in close collaboration with internal stakeholders to assist in the implementation of scientific initiatives focused on both internal and external customers. • Ensure accurate, timely and current medical updates to scientific communications materials and resources in use by FMA Team related to current and future treatment modalities and guidelines. • Create, review, update and archive FMA slide libraries, new hire material, therapeutic/product-specific key studies and other appropriate scientific/clinical material for use by FMA. • Serve as internal stakeholder to the Medical Omnichannel Team in creation of scientific statements, digital assets, etc. in support of therapeutic/product specific strategies. • Act as a liaison among FMA team, respective TA, MedMod&SPE, and Medical Information Departments. • Develop and implement MA assessment strategies and tools to evaluate FMA scientific competencies and knowledge level. • Manage relationships, contracts and projects with vendors and ensure projects are completed on time and within budget.

🎯 Anforderungen

• A Doctoral degree (PharmD, PhD or MD/DO) required • A minimum of 3 years of Field medical experience or prior work experience in a similar role required • A minimum of 5 years of industry experience required • Ability to manage multiple projects and engage stakeholders in a dynamic environment with tight timelines • Demonstrated understanding of legal and regulatory environment of pharmaceutical industry • Possess strategic thinking and problem-solving skills • Possess superior communication skills, both oral, written and presentation, and ability to engender trust and respect of peers and superiors • Presentable, highly articulate, goal-oriented, honest, with high integrity and strong ethics • Prior experience in diabetes and/or obesity preferred • Proficiency in Microsoft PowerPoint, Excel and Word software applications and overall advanced computer skills with knowledge of literature search techniques required • Proven track record of strong teamwork, innovation, and project management

🏖️ Vorteile

• medical, dental and vision coverage • life insurance • disability insurance • 401(k) savings plan • flexible spending accounts • employee assistance program • tuition reimbursement program • voluntary benefits such as group legal, critical illness, identity theft protection, pet insurance and auto/home insurance • time off including sick leave, vacation policy, and parental leave policy