Black Diamond Therapeutics is a next-wave cancer precision medicine company. We are dedicated to revolutionizing the field of oncology by developing selective medicines for patients with genetically defined cancers driven by oncogenes activated by allosteric mutations. Our innovative mutation, allostery, and pharmacology (MAP) computational and discovery platform enables us to functionally assess the mutational landscape of individual oncogenes, leading to the discovery and validation of new targets. Through our research and development efforts, we aim to develop highly selective therapeutics that offer new hope to cancer patients.   Scope: As a Senior Medical Science Liaison, you will play a critical role in establishing and maintaining scientific relationships with key external stakeholders, including healthcare professionals, academic institutions, and advocacy groups. You will serve as a scientific expert, providing comprehensive and accurate information on our programs and the therapeutic landscape in oncology. Your primary responsibility will be to educate and collaborate with healthcare professionals to ensure optimal patient care and support Black Diamond's mission to advance precision medicine for cancer.   This territory will be responsible for either the East or West half (live or virtual) of the United States with some international coverage.

Black Diamond Therapeutics is a next-wave cancer precision medicine company. Black Diamond is at the forefront of developing selective medicines for patients with genetically defined cancers driven by oncogenes activated by allosteric mutations. Leveraging its innovative mutation, allostery, and pharmacology (MAP) computational and discovery platform, Black Diamond is revolutionizing the field by uncovering novel ways to functionally assess the mutational landscape of individual oncogenes. This approach allows us to discover and validate new targets and develop highly selective therapeutics that offer new hope to cancer patients.   Scope: This is a critical role in writing and reviewing complex clinical and scientific documents in a clear, concise, and engaging manner for a variety of audiences, including regulatory agencies and internal stakeholders. Your ability to effectively communicate scientific information will contribute to the advancement of our innovative oncology precision medicine programs.

Company Overview: Black Diamond Therapeutics is a next-wave cancer precision medicine company. Black Diamond is at the forefront of developing selective medicines for patients with genetically defined cancers driven by oncogenes activated by allosteric mutations. Leveraging its innovative mutation, allostery, and pharmacology (MAP) computational and discovery platform, Black Diamond is revolutionizing the field by uncovering novel ways to functionally assess the mutational landscape of individual oncogenes. This approach allows us to discover and validate new targets and develop highly selective therapeutics that offer new hope to cancer patients.   Scope: The Sr. Manager, Data Management will play a critical role in leading our data management activities, ensures that program and study level deliverables are completed on time, with a high degree of quality, and in accordance with corporate and regulatory requirements. This position requires a strong background in data management, excellent leadership skills, and the ability to collaborate with cross-functional teams. The successful candidate will contribute to data management oversight, data delivery, and ensure regulatory compliance.

Scope The Executive Director (ED)/Vice President (VP), Regulatory Affairs will lead and oversee the Black Diamond global regulatory strategy across all stages of development (preclinical, clinical, and commercialization) for oncology products, including both clinical, companion diagnostics (device), and CMC regulatory activities. This role will require direct hands-on contributions, as well as oversight of the growth and supervision of the Company’s regulatory organization, which may include senior regulatory strategists (clinical and CMC), regulatory publishing/submissions, regulatory intelligence, and regulatory archives.                                                                    The ED/VP, Regulatory Affairs will be an active member of the Development Operations Leadership Team to support overall functional infrastructure, resourcing, and annual goal development across Development Operations.    In addition to Regulatory Affairs functional responsibilities, this role will be involved in strategic development discussions providing Regulatory Affairs leadership and support in the development of global clinical development plans and regulatory submission strategies. This role may be an active member (or oversee the Regulatory core team members) of the products’ Program Teams and will lead the Regulatory Subteam across all development programs to align on regulatory strategies and risks to communicate to the Program Teams and Executive Leadership Team (ELT).