Senior Biomarker Program Manager

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

AbbVie strongly believes in the importance of identifying patients who are most likely to benefit from the medicines that they develop and commercialize. To this end, AbbVie has established and expanded core capabilities in Precision Medicine (PMed), encompassing clinical trial management, translational medicine and companion diagnostics. Within PMed, the Biomarker Program Management (BPM) team connects science and operations to manage biomarker research for multiple Phase 1-3 clinical trials. We are seeking an experienced and highly motivated individual who will employ operational and logistical strategies to ensure clinical trials are executed with quality and efficiency, on-time, within budget, and meet objectives. The successful candidate will have a proven track record of clinical trial experience and decision-making to achieve these objectives, including scientific expertise, strategic thinking, a patient-oriented mindset, team building and cross-functional collaboration.

Responsibilities:

• Manage biomarker operations and logistics to support the clinical trial schedule, ensuring data are ready for analysis per timeline. Resolve or escalate biomarker study-related issues with PMed Lead or BPM Subject Matter Expert (SME).
• Responsible for relevant biomarker content in clinical study documents and associated systems (including clinical trial blueprint/protocol, informed consent forms, eCRFs, CSRs, etc). Responsible for generating study related training materials for the study team, study sites and vendors for each trial. Ensure consistency across programs.
• Manage EC/IRB biomarker related inquiries, ensuring consistent responses across studies while maintaining AbbVie biomarker sta