An exciting leadership role is open for an experienced Clinical Research Site Director to guide operations at a dedicated hematology/oncology research facility in Los Angeles. This is a unique opportunity to influence the development of cutting-edge cancer therapies and improve outcomes for patients across the globe. In this role, you’ll oversee a team of clinical research professionals, manage sponsor relationships, and ensure full compliance with FDA/21 CFR and ICH-GCP guidelines. Your leadership will be key in advancing oncology and hematology studies that have a real-world impact. We’re looking for a strong clinical operations leader with in-depth knowledge of oncology trials. Ideal candidates bring proven experience managing research teams, deep regulatory understanding, and a passion for contributing to meaningful advancements in cancer care. Your Focus Will Include: • Managing daily operations and supervising research staff • Collaborating with sponsors to align study objectives and timelines • Ensuring compliance with regulatory and ethical standards • Promoting high-quality participant care and engagement • Tracking site metrics and driving timely trial execution If you're ready to step into a pivotal leadership role in cancer research, we’d like to hear from you. Join a mission that matters. Responsibilities: • Site Management : Oversee daily operations of the clinical research site, including study planning, protocol implementation, patient recruitment, data collection, and maintaining regulatory compliance. • Team Leadership : Manage and mentor a team of approximately 15 Clinical Research Coordinators and 10+ Research Assistants. Provide guidance and training and conduct performance evaluations to ensure high-quality work and adherence to compliance standards. • Regulatory Compliance : Ensure all clinical research activities comply with Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and other relevant regulatory requirements. • Study Execution : Serve as the subject matter expert for sponsors and research organizations, collaborating with the Principal Investigator (PI) to oversee compliance of clinical trial teams in accordance with protocols, timelines, and budgets. • Patient Recruitment & Retention: Work closely with the recruitment team to develop effective strategies for research participant recruitment and retention, ensuring access to eligible participants and maintaining participant engagement throughout the study. • Budget & Financial Oversight: Manage study budgets, invoicing, and site expenditures, ensuring effective use of resources while staying within allocated financial parameters. • Quality Assurance : Ensure data integrity by reviewing audit trails, identifying compliance or quality concerns, and implementing corrective actions. Monitor ongoing site performance to detect risks and take proactive measures. • Collaboration & Communication: Foster strong communication and collaboration between internal teams, study sponsors, and external stakeholders, ensuring alignment and transparency in the study’s progress. • Clinical Data Management : Oversee the collection and review of clinical data, ensuring strict compliance with study protocols and regulatory requirements. Qualifications: • Education : Bachelor's degree in life sciences, nursing, or a related field (required). A Master's degree or higher is preferred. • Experience : Minimum of 5 years of clinical research experience, with at least 2 years in hematology/oncology clinical trials. A minimum of 3 years in a management or leadership role overseeing clinical research teams (CRCs and RAs). • Certifications : CCRP (Certified Clinical Research Professional), CCRC (Certified Clinical Research Coordinator), or other relevant certifications preferred. • Knowledge : In-depth understanding of clinical research methodologies, regulatory compliance (FDA, ICH-GCP), and hematology/oncology drug development. • Skills : Strong leadership, communication, organizational, and problem-solving skills. Proficiency in clinical trial management systems and Microsoft Office Suite. • Other: Ability to manage multiple priorities in a fast-paced environment while maintaining high standards of performance and patient care. Compensation: The salary for this position is competitive and positioned within the 80th to 90th percentile for Clinical Research Site Directors in the Los Angeles area, based on experience and qualifications. A comprehensive benefits package is included, covering health, dental, and vision insurance, 401(k), and paid time off. Work Environment: • The Clinical Research Site Director will primarily work in a clinical research setting, interacting with patients, site staff, and external stakeholders. • Occasional travel to sponsor meetings or other clinical sites may be required. • Full-time position with flexible hours based on study needs. Compensation: $145,000 - $165,000

• Site Management: Oversee daily operations of the clinical research site, including study planning, protocol implementation, patient recruitment, data collection, and maintaining regulatory compliance. • Team Leadership: Manage and mentor a team of approximately 15 Clinical Research Coordinators and 10+ Research Assistants. Provide guidance and training and conduct performance evaluations to ensure high-quality work and adherence to compliance standards. • Regulatory Compliance: Ensure all clinical research activities comply with Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and other relevant regulatory requirements. • Study Execution: Serve as the subject matter expert for sponsors and research organizations, collaborating with the Principal Investigator (PI) to oversee compliance of clinical trial teams in accordance with protocols, timelines, and budgets. • Patient Recruitment & Retention: Work closely with the recruitment team to develop effective strategies for research participant recruitment and retention, ensuring access to eligible participants and maintaining participant engagement throughout the study. • Budget & Financial Oversight: Manage study budgets, invoicing, and site expenditures, ensuring effective use of resources while staying within allocated financial parameters. • Quality Assurance: Ensure data integrity by reviewing audit trails, identifying compliance or quality concerns, and implementing corrective actions. Monitor ongoing site performance to detect risks and take proactive measures. • Collaboration & Communication: Foster strong communication and collaboration between internal teams, study sponsors, and external stakeholders, ensuring alignment and transparency in the study’s progress. • Clinical Data Management: Oversee the collection and review of clinical data, ensuring strict compliance with study protocols and regulatory requirements.