Senior Medical/Scientific Director, Medical Affairs -Multiple Myeloma

Allergan; Lincoln (NE); Hybrid; USD 150,000 - 210,000; Full time

Job summary

An established industry player is looking for a Senior Director to provide strategic medical and scientific input into core medical affairs activities. This role involves collaboration with marketing and commercial teams to influence brand strategies and drive scientific communication initiatives. The ideal candidate will have extensive experience in clinical trials and regulatory requirements, ensuring that patient safety is prioritized. Join a forward-thinking organization that values innovation and has a significant impact on healthcare solutions.

Qualifications

• Minimum 5 years clinical trial experience in biotech/pharma.
• Proven leadership in managing clinical programs independently.

Responsibilities

• Lead medical affairs activities for multiple myeloma.
• Oversee development of marketing materials and medical education programs.

Skills

Leadership

Clinical Trial Methodology

Regulatory Requirements

Stakeholder Engagement

Scientific Communication

Education

MD or equivalent

PhD or PharmD

Job description

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that address serious health issues today and future medical challenges. We aim to have a significant impact on people's lives across key therapeutic areas such as immunology, oncology, neuroscience, and eye care, including products and services in our Allergan Aesthetics portfolio. For more information, visit www.abbvie.com. Follow us on X, Facebook, Instagram, YouTube, LinkedIn, and TikTok.

Job Description

*Hybrid work preferred in Lake County, IL, Florham Park, NJ, or San Francisco, CA. Remote candidates will also be considered.

*Position title will depend on qualifications listed below.

Purpose:

The Senior Director provides strategic and operational medical and scientific input into core medical affairs activities, including healthcare professional interactions, data generation, educational initiatives, and safeguarding patient safety. Collaborates closely with marketing and commercial teams to influence brand strategies, medical/marketing activities, and market access. Leads external stakeholder engagement and drives scientific communication initiatives.

Responsibilities:

• Lead medical affairs activities for multiple myeloma, collaborating with global teams and cross-functional partners to develop and execute strategic plans.
• Oversee development of scientifically accurate marketing materials, medical education programs, and advisories.
• Manage medical governance for relevant products and develop integrated evidence plans.
• Initiate and support research projects, develop scientific communication platforms, and provide training to internal teams.
• Build and maintain relationships with key opinion leaders and participate in cross-functional teams to align medical strategies.
• Contribute to clinical trial design, safety reporting, and the development of educational programs.
• Represent Medical Affairs in due diligence activities and ensure compliance with budgets and timelines.

Qualifications

Senior Medical Director:

• MD or equivalent, with clinical trial experience in biotech/pharma or academia (minimum 5 years, preferred 7+).
• Proven leadership and ability to manage clinical programs independently.
• Extensive knowledge of clinical trial methodology, regulatory requirements, and therapeutic areas.

Senior Scientific Director:

• PhD or PharmD, with 10-15 years of industry experience, including clinical trial and medical affairs expertise.
• Strong leadership skills and knowledge of clinical development and regulatory processes.

Additional Information

Details on compensation, benefits, and legal notices are provided, including pay range disclosures and equal opportunity statements. Applicants in applicable locations will be considered for incentives and benefits as described.