Associate Medical Director, Medical Affairs - Hematology

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 Tik Tok.

Job Description

*Hybrid 3x per week in Lake County, IL, Florham Park, NJ or San Francisco, CA. Will consider remote candidates.

The Associate Medical Director provides specialist medical/scientific strategic and operational input into core medical affairs activities within hematology oncology inclusive of healthcare professional/provider interactions; generation of clinical and scientific data; educational initiatives (medical education, data, guidelines and value proposition); safeguarding patient safety (risk minimization activities / safety surveillance activities). Works closely with colleagues (e.g. Clinical, safety, marketing) to provide strategic medical input into core brand strategies. Provides scientific and technical support for assigned products; delivers scientific presentations; develops and maintains professional and credible relationships with key opinion leaders; actively participates in relevant Brand Teams and helps develop medical affairs strategies for assigned products. Develops innovative research concepts for clinical data generation and provides relevant scientific and technical training. 

Responsibilities: 

• Develops, reviews and follows up on clinical studies and medical projects initiated within the relevant therapeutic area (e.g. post marketing clinical activities such as real-world/database projects, epidemiological surveys, secondary analyses, post-authorization studies (phase IV), IIS projects, etc.). 

• Participation in design and execution of clinical trial safety, product safety and risk management plans. Responsible for routine and adhoc safety monitoring reports to regulatory agencies. May review, assess and report applicable Adverse Events (AE’s) an