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Director, Clinical Scientist

🔥 2 minutes ago

🏄 California – Remote

infoinfo

💵 $190k - $225k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

Where this job comes from

Posted on Kumquat Biosciences Inc.'s careers page, not through a job board

First seen by Remote Rocketship 2 minutes ago

Logo of Kumquat Biosciences Inc.

Kumquat Biosciences Inc.

11 - 50 employees

🏥 Healthcare

🧬 Biotechnology

⚕️ Healthcare Insurance

💰 $70M Corporate Round on 2021-07

Healthcare • Biotechnology • Healthcare Insurance

Kumquat Biosciences Inc. is a biotechnology company dedicated to innovating life-changing medicines for cancer patients. With a focus on the KRAS pathway, Kumquat develops both single and combination therapies that target previously undruggable cancer types and stimulate the immune system to enhance therapeutic outcomes. Through a culture of bold innovation and collaboration, they strive to set new standards in cancer treatment, bringing the latest advancements from research to patient care.

📋 Description

• 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 study teams • Contribute to clinical and regulatory documents including Clinical Study Reports, informed consent forms, Investigator’s Brochures, and DSURs • Serve as a partner to external stakeholders in various countries and support local needs • Maintain up-to-date knowledge of the emerging treatment landscape in study-specific areas • Cultivate peer-to-peer collaborations and support patient-centric study operations • Work with colleagues across Kumquat to promote communication, community, and growth opportunities • Ensure GCP/GVP compliance, data integrity, and a balanced risk-based approach • Provide subject matter expertise supporting the design and execution of clinical trials and enabling projects across geographies • Contribute to the outcomes of clinical trials and enabling projects • Apply ICH, GCP, and regulatory guidelines within clinical trials or enabling activities • Participate in identifying vendors, building relationships with sites and investigators, and supporting trial execution • Work closely with investigators 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)

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