Job
Description
The Associate Clinical Development Director (Assoc. CDD) plays a crucial role in contributing to the development of protocols for assigned global clinical trials, monitoring scientific aspects, and ensuring the reporting of high-quality data. Depending on the size and complexity, they may also provide support in developing the clinical and scientific strategy for specific sections of a clinical development program. Their responsibilities encompass overseeing all operational aspects of clinical trials, from planning and execution to interpreting research findings and managing data collection activities and clinical operations. Additionally, they are responsible for complete oversight of budget and resource allocation within the assigned trial, driving operational excellence through process improvement and knowledge sharing across trials within the program or franchise. The Associate Clinical Development Director serves as a point of escalation for resolving operational issues within the assigned trial. In their role, the Associate Clinical Development Director is tasked with providing input to the development of clinical development strategy, contributing to the development of trial-related documents, and collaborating with the appropriate Clinical Trial Team (CTT) members. They conduct ongoing scientific reviews of clinical trial data, manage patient safety reports, provide input into final analyses and interpretations, and contribute to global initiatives for process improvement and other line function activities. The Associate Clinical Development Director may also lead clinical trials as a Clinical Scientific Lead, providing leadership and guidance for all clinical aspects of the trial in collaboration with the medical monitor and/or Clinical Development Director. Key Performance Indicators for the role include demonstrating quality clinical and scientific strategic input, applying effective clinical research methodology, supporting Therapeutic Area (TA) through high-quality contributions, and ensuring timely development of disease/program clinical standards, publications, and presentations. The Associate Clinical Development Director is expected to excel in executing and implementing clinical operations strategy, managing budget and resources effectively, and demonstrating strong leadership skills to support team competency building and best practice sharing across programs and departments. Clear communication of risks, cost-effective management, and adherence to Novartis Values and Behaviors are also essential aspects of the role. Minimum Requirements for the position include a preference for Neuroscience or similar experience, an advanced degree in life sciences or healthcare, and at least 3 years of involvement in clinical research or drug development in an academic or industry environment. The ideal candidate should have a working knowledge of clinical trial design and methodology, statistics, regulatory processes, and strong communication and interpersonal skills. Proficiency in budget management, clinical research, coaching, cross-functional teamwork, and risk management is also necessary. Language requirements for the role include proficiency in English. Novartis offers a collaborative environment for individuals passionate about making a difference in patients" lives through innovative science. If you are ready to contribute to creating a brighter future, consider joining the Novartis Network to explore career opportunities and benefit from a supportive community focused on personal and professional growth.,
