Senior Medical/Scientific Director, Medical Affairs -Multiple Myeloma

Allergan; Greenlawn (NY); Hybrid; USD 120,000 - 220,000; Full time

Job summary

An established industry player seeks a Senior Director to provide strategic medical input and leadership in core medical affairs activities. This role involves collaboration with marketing and commercial teams, overseeing the development of scientifically accurate materials, and managing clinical trial governance. The ideal candidate will have extensive experience in clinical trials and a strong background in medical affairs. Join a forward-thinking company dedicated to addressing serious health issues and making a significant impact on patient care through innovative solutions.

Qualifications

• 5+ years clinical trial experience required, with a preference for 7+ years.
• Proven leadership and team management skills essential.

Responsibilities

• Lead the development of marketing materials and medical education programs.
• Manage medical governance for products and develop integrated evidence plans.
• Coordinate team development and provide scientific support.

Skills

Leadership

Clinical Trial Management

Strategic Medical Input

Regulatory Requirements Knowledge

Therapeutic Area Expertise

Education

Medical Doctorate (M.D.)

PhD or PharmD

Job description

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn, and TikTok.

Job Description

*Hybrid in Lake County, IL, Florham Park, NJ or San Francisco, CA preferred. Will consider remote candidates.

*Position title will be based on qualifications listed below.

Purpose:

The Senior Director provides specialist medical and scientific strategic and operational input into core medical affairs activities such as healthcare professional/provider interactions (Payers, Patients, Prescribers, and Providers); generation of clinical and scientific data; educational initiatives; safeguarding patient safety; and market access. Works closely with marketing and commercial teams to provide strategic medical input into core brand strategies, and to drive medical/marketing activities and market access. Leads or contributes to asset strategy development and external stakeholder interactions, including scientific communication initiatives.

Responsibilities:

• Provide leadership and support for multiple myeloma, collaborating with various functional teams to execute medical activities and provide strategic input.
• Lead the development of scientifically accurate marketing materials, medical education programs, and advisories.
• Manage medical governance for products and develop integrated evidence plans.
• Initiate and support data generation, develop research concepts, and provide scientific training.
• Coordinate team development and provide scientific support, including presentations and key opinion leader relationships.
• Contribute to trial design and review safety data in clinical studies.
• Lead advisory boards and medical education programs, and stay current with professional developments.
• Represent Medical Affairs in due diligence activities for asset acquisition.
• Manage budgets, timelines, and compliance for scientific programs.

Qualifications

Senior Medical Director:

• Medical Doctorate (M.D.) or equivalent; residency/fellowship preferred; licensed to practice medicine preferred.
• Minimum 5 years clinical trial experience; 7+ years preferred.
• Proven leadership and team management skills.
• Extensive knowledge of clinical trials, regulatory requirements, and therapeutic areas.

Senior Scientific Director:

• PhD or PharmD; postdoctoral experience preferred.
• 15+ years in the industry; 10+ years in clinical trials or medical affairs.
• Proven leadership and expertise in therapeutic areas.

Additional information about compensation and company policies is included, along with equal opportunity statements and links for accommodations.