Over 6 million people in the US are affected by Heart Failure in the US with that number expected to increase to 8 million by 2030. Novartis has been at the forefront of cardiovascular treatment for decades, delivering groundbreaking medicines that extend and improve life, and that's where we intend to stay.
The CDMD oversees the planning, execution, and interpretation of clinical trials research, data collection activities and clinical operations. Establishes and approves scientific methods for design and implementation of clinical protocols, data collection systems and final reports. Support new and ongoing clinical research and clinical trials and ensure efficient and timely processing of confidentiality agreements and clinical agreements.
Your responsibilities will include:
-Acts as a clinical leader for a region / large countries or strategic sites responsible for assigned clinical program(s) -driving medical strategy implementation and operational deliverables for development and marketed products in a defined therapeutic area . -Provides clinical leadership and strategic guidance for all clinical deliverables in the assigned section of a clinical program and/or programs. -Ensure effective cross-functional communications to align with global strategy -Leads development of clinical sections of trial and program level regulatory documents -Drives execution of the section of the clinical program in partnership with global line functions. -Supports the clinical research leaders by providing medical input into IDP and CTP reviews and contributing/driving development of disease clinical standards for new disease areas -Acts as the medical expert, engages interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, data monitoring committees, advisory boards etc.) and internal NVS stakeholders.