Associate Medical Director, Leukemia & Lymphoma Job in San Jose, California US
Fantastic opportunity to join global market leader in biotech and medical devices in Associate Medical Director role.
The Associate Medical Director, L&L, reports to the VP Medical Affairs and Clinical Operations and is responsible for overseeing all Clinical Operations and Medical Affairs activities associated to ongoing and future L&L clinical programs.
The Clinical Operations activities will include supporting the L&L clinical projects, clinical study designs and clinical trials in conjunction with the Director of Clinical Operations.
Additionally, the Associate Medical Director is responsible for strategic interactions with R&D, Marketing, Regulatory Affairs and Core teams and provides medical input, perspective and vision to the senior leadership team.
The Medical Affairs activities will include interactions with key experts and opinion leaders in hematopathology (e.
g., Investigator Initiated Studies), professional societies, as well as defining and executing a strategy for scientific publications and product investigations.
Primary Responsibilities: In collaboration with the VP Medical Affairs and Clinical Operations, oversee the management of all aspects of Medical Affairs and Clinical Operations in the L&L field.In collaboration with the Director of Clinical Operations, ensure delivery of optimal outcomes in L&L clinical trials, meeting objectives on-time, within budget and of the highest quality.
Provide ongoing strategic insight to the leadership team regarding research and industry trends and business opportunities.
Provide training and support to the organization related to clinical and relevant commercial aspects in L&L and ensure high quality scientific and core message integrity.
Lead and coordinate Investigator Initiated Studies in support of product positioning, market development, relevant basic and clinical research, including review of protocols and draft publication manuscripts.
Actively participate in functional and cross-functional meetings and contribute to the development of current and anticipated business opportunities.
Serve as the company's hematopathology expert at external scientific and industry meetings.
Qualifications: PhD or MD degree5 years of hematology/hematopathology in a lab environment3 years of experience utilizing and interpreting flow cytometry data2 years of experience overseeing or conducting clinical trials Minimum of 1 year experience managing othersLocal Candidates only, no relocation provided.
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