On this Business of Biotech podcast, Cullinan Oncology CEO Nadim Ahmed shares the story of his company’s drug discovery efforts, which have yielded a wide range of multimodal candidates spanning a range of cancer indications. Our discussion digs into the company's transition from R&D to the clinic, how it has built an uncommonly comfortable cash position through partnership, and its ambition to become a fully integrated commercial-stage biotech. Listen now!
At a certain point in your career, you realize that while you have a wealth of knowledge and experience, you’re not making the impact you want to have. What you are lacking is executive presence, and that will directly undermine your value at work.
While people don’t always think about the choreography of good scientific teamwork, there are factors that should be considered and skills that can be developed to increase a drug discovery team’s overall effectiveness and chance of success.
Join Camila Matheny, DCT implementation expert, as she discusses the benefits of adopting consent management technology and provides best practices around developing change management and training programs to help sponsors, CROs, and sites get the most out of eConsent. Click here to learn more.
The European Union Clinical Trial Regulation No. 536/2014, which went into effect in January, introduced the most significant changes to the processes for clinical trial applications in at least the past 15 years. Learn how it impacts the Trial Master File and consider three key functions that an electronic TMF must have to achieve compliance and maintain organizational success.
Discover challenges for drug makers who may want to produce higher potency APIs but have built their manufacturing systems around broad-spectrum medications that don’t require high-containment facilities.
The decision whether to develop and manufacture a drug in-house or to outsource comprises numerous elements, including costs, timelines, production capacity, and available resources.
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