Description The Director, Clinical Scientist is an integral member of a cross-functional team for a study drug from first in human to registration by providing input and execution of the clinical development plan by helping develop and execute protocols and protocol amendments. Key Responsibilities • Perform ongoing clinical data review and analysis to ensure data integrity, identify trends, and support safety and efficacy assessments • Review and interpret clinical data to identify trends, investigate unexpected findings, and provide meaningful insights to study teams • Support medical monitoring activities, including review of adverse events, protocol deviations, and long-term safety and efficacy outcomes • Provide input and execution of the clinical development plan by helping to develop and execute protocols and protocol amendments • Actively participate in study/site start-up activities, site engagement (including SIVs and committees), and provide general clinical support to the study teams • Contribute to key clinical and regulatory documents including Clinical Study Reports (CSRs), informed consent form(s), Investigator’s Brochures (IBs), and DSURs • Serve as a partner to external stakeholders in various countries and help support local needs • Manage up-to-date knowledge on the emerging treatment landscape in study specific areas • Cultivate meaningful peer-to-peer collaborations and nurture a culture of curiosity to enable faster, simpler, and more patient-centric ways of operating our studies • Work with colleagues across Kumquat to promote communication and community. Optimizing growth opportunities and capabilities to successfully contribute and operate in a diverse and global environment. Drive new thinking by identifying new opportunities and options to embrace value creation. • Ensure GCP/GVP compliance, data integrity, and take a balanced risk-based approach in the work you are focused on, seeking guidance or direction as needed. • Provides subject matter expertise on activities or through supporting the design and execution of clinical trials and/or enabling projects across geographies. • Contributes to the outcome of one or more clinical trials and/or enabling projects. • Understands, applies proficient knowledge of, and ensures adherence to ICH, GCP, and regulatory guidelines within clinical trials or enabling activities. • Participates in identifying vendors, builds relationships with sites and investigators and partners to ensure the execution of clinical trials. • Work closely with Investigator and clinical site staff Requirements • BS/BA with advanced degree preferred • Oncology and or hematology focus • At least 5 years of relevant experience either in the pharmaceutical industry, community setting or academia. • Phase 1 study trial experience in either solid tumor or hematologic malignancies with a focus on small molecules preferred • Working knowledge of Drug Development and Clinical development activities and deliverables. • Ability to solve complex outcomes; takes a new perspective on existing solutions; exercises judgment based on analyzing multiple sources of information and advice. • Ability to travel up to 10% of the time domestically or internationally • Excellent problem-solving skills and proven track record of delivering to aggressive timelines • High ethical and professional standards, working in accordance with regulations and company policies and procedures • Proficient use of MS Office (Word, Excel, PowerPoint)