Program Development & Training Director

🕒 May 21

🏖️ New Jersey – Remote

🏖️ New Jersey – Remote

💵 $187.1k - $327.5k / year

⏰ Full Time

🔴 Lead

👔 Director

🦅 H1B Visa Sponsor

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Novo Nordisk

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1923

⚕️ Healthcare Insurance

💊 Pharmaceuticals

🧬 Biotechnology

Healthcare Insurance • Pharmaceuticals • Biotechnology

Novo Nordisk is a global healthcare company that has been at the forefront of research in obesity and diabetes for over 25 years. Their mission is to improve the lives of people suffering from obesity and diabetes through innovative treatments and sustainable practices. With a strong commitment to patient safety, Novo Nordisk actively combats falsified medicines and strives to enhance the integrity of their products. They offer a range of life-saving medications and are dedicated to driving change in the healthcare landscape, ensuring that children and adults alike have access to essential medical care.

📋 Description

• 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.

🎯 Requirements

• 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

🏖️ Benefits

• 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