Senior Director, Clinical Data Management and Analytics

Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview Senior Director, Clinical Data Management and Analytics, provides leadership to the Clinical Data Management and Analytics Department and provides influence across the Clinical Development organization. As a leader of the Clinical Data Management and Analytics organization, and part of a cross-functional team of drug development scientists focused on providing hands on skills, expertise, and tools to facilitate strategic development, operational execution, and regulatory compliance to ensure data integrity for clinical trials, in addition to integration, visualization, and exploratory analysis of complex and diverse data in support of clinical development activities and decisions. Through practical hands-on work, the Lead will define approaches, processes, algorithms, and tools that support the analytics, visualizations, and decision support needs of drug development scientists and projects. The Lead will play a key role in building the team with the necessary skills, build relationships with relevant stakeholders, and implement relevant tools and approaches. The Lead will collaborate with Biostatistics leads and other members of drug development teams to ensure connectivity of exploratory analysis work in support of development, regulatory approval, and market acceptance of products. This position includes functional management responsibilities. Essential Functions and Responsibilities Define and implement the overall vision, strategy, and goals for the clinical data management department. Lead, manage, and develop data management teams, handling resource planning, staff training, and performance reviews. Ensure data integrity, quality, and compliance with regulatory requirements (e.g., FDA, ICH, GCPs) and internal company policies. Experience with global trials and regulatory submissions (FDA, EMA). Generate novel insights from data and present them via rich and intuitive visualizations. Builds successful partnerships and seamless interfaces within the department and the broader research and development organization. Communicates proactively and effectively across several teams with diverse subject matter expertise. Ensures quality of deliverables by consistently applying analysis and reporting standards, and driving compliance with regulatory requirements, corporate and departmental SOPs, and work practices. Drives the development and implementation of innovative strategies and technologies. Independently develops, troubleshoots, and maintains complex programs and utilities in accordance with predefined specifications and build upon existing Iovance standards. Provides technical guidance to external partners concerning project and data standards, and analysis practices to ensure efficient and integrated project strategies. Identifies opportunities for increased efficiency and consistency within the organization and provides SME support to continuous improvement initiatives. Adheres to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics. Performs miscellaneous duties as assigned. Required Education, Skills, and Knowledge Extensive experience in clinical data management and systems, with proven leadership experience in oncology therapeutic area. Proficient knowledge of EDC systems (e.g., Medidata Rave), CDISC standards, and clinical trial processes. Drive innovation and continuous process i ... (truncated, view full listing at source)