Senior Medical/Scientific Director, International Medical Affairs - Multiple Myeloma

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

The Senior Medical Director provides specialist medical/scientific strategic and operational input into core medical affairs activities within the designated therapeutic area.

• This will include 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 commercial teams to provide strategic medical input into core brand strategies, and to support medical/marketing activities and market access.
• 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; provide relevant scientific and technical training.

Responsibilities:

• Establishes and approves scientific methods for hypotheses, rationale, design of study protocols and their reports across different products.
• Oversees the conduct of clinical trials and is medically and scientifically accountable for resolution of safety issues, interpretation of statistical analyses for clinical significance, PI selection, scientific documents reporting safety monitoring and other scientific reports submitted to the regulatory authorities.  
• Participation in design and execution of clinical trial safety, product safety and risk management plans.  May also carry responsibility fo