The Vice President of Global Clinical Development is tasked with steering the strategic planning and execution of worldwide clinical programs for oncology. This role is crucial for shaping the clinical pipeline and achieving regulatory milestones.
The client offers a dynamic international environment that integrates research and development, regulatory, commercial, and clinical operations. The focus is on delivering innovative oncology and autoimmune therapies to meet unmet medical needs globally, with a strong trajectory towards conducting global clinical trials and commercialization.
Key responsibilities include developing and implementing strategies for global clinical development, overseeing the design and execution of clinical trials, and handling regulatory submissions in a timely and compliant manner. The role involves leading and mentoring a high-performing clinical development team, enhancing processes, and collaborating with both internal stakeholders and external partners, such as investigators, key opinion leaders, and regulatory agencies.
Additionally, the position requires representing the client at major scientific meetings and regulatory interactions, thereby ensuring the company maintains its leadership in the field.
Ideal candidates for this role hold an M.D., with over 15 years of relevant clinical development experience, particularly in oncology or autoimmune diseases. They should have a proven track record in managing global Phase I-III trials and engaging with regulatory bodies like the FDA. Leadership experience, strategic thinking, and cross-functional leadership skills are essential, along with strong communication and negotiation abilities.
The role offers a competitive executive package with opportunities for career growth in a high-impact and rapidly evolving sector.