What are the responsibilities and job description for the Senior Medical Director (Hematology) position at F. Hoffmann-La Roche AG?
Senior Medical Director (Hematology)
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Locations : Shanghai, Beijing
Time Type : Full Time
Posted on : Posted 30 Days Ago
Job Requisition ID : 202412-131750
Roche fosters diversity, equity, and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people’s varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice matters.
The Position
This Opportunity
Roche’s Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development (Phase II – III) clinical strategies and plans that deliver medically-differentiated therapies that provide meaningful improvement to patients. The Senior Medical Director leads development of the Clinical Development (CD) strategy and plan and is responsible for ensuring effective and efficient execution for the assigned molecule(s) / indication(s). Senior Medical Directors are expected to demonstrate mastery of the core Medical Clinical Director role, perform their responsibilities mostly independently, and effectively lead multiple projects.
EXPERIENCE AND QUALIFICATIONS :
- M.D. Required
- Relevant clinical, scientific, or clinical trial / development experience in same / similar therapeutic area required
- Academic / teaching background is a plus
- Extensive experience working with the principles and techniques of data analysis, interpretation, and clinical relevance
- Experience publishing results of a clinical trial in a peer-reviewed journal is required
- Extensive pharma / biotech industry experience OR is a recognized expert in the field with significant clinical research experience
- Extensive experience designing and conducting clinical trials (i.e. multiple trials)
- Experience authoring a global clinical development plan is required
- Advanced understanding of Phase II – III drug development
- Knowledge and understanding of Phase I & IV drug development is preferred
- Comprehensive understanding of product and safety profiles
- Advanced understanding of medical aspects of GCP (Good Clinical Practice), ICH (International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use), FDA, EMA, and other relevant guidelines and regulations is required
- Experience leading a HA interaction and submitting an NDA / BLA / MAA to HAs in the US and / or Europe is preferred
- 6 or more years pharma / biotech experience OR recognized expert in field OR is the equivalent of an Associate Professor. A minimum of 2 years industry experience is strongly preferred
- Prior people management experience is preferred
- Up to 30% global travel
Key Skills and Behaviours
SPECIFIC DUTIES AND RESPONSIBILITIES :
Who we are
At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity, and diversity.
Roche is an Equal Opportunity Employer.
About Us
We believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are passionate about transforming patients’ lives. We are courageous in both decision and action. And we believe that good business means a better world.
We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow.
We are proud of who we are, what we do, and how we do it.
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