Associate Director Study Leader, Oncology R&D, Early Oncology Clinical

.Location: Barcelona, Spain (On-site): We require 3 days working from the office and 2 days working from home.Join our Oncology R&D team as an Associate Director Study Leader, where you will be responsible for the delivery of clinical studies, ensuring quality, timelines, budgets, resources, and key project deliverables are met in compliance with SOPs, Regulatory requirements and ICH/GCP guidelines. This role provides matrix management of functional area representatives to cross-functional clinical study teams. The exact accountabilities will differ depending on the exact nature of the clinical program so a high degree of flexibility is required.Typical Accountabilities:Leads the delivery of the clinical study from concept to final CSR and through to study closure and archive to agreed budget, time, project standards, quality and scientific standardsMay convene and lead the cross functional study team(s) for Early Oncology Clinical studies based on delivery modelLead and optimize the performance of study delivery teams ensuring GCP compliance, including provision of timely and accurate performance feedback for study team members to the appropriate AZ manager or CRO representativeContribute to preparation and delivery of study documents (e.G. Protocols/amendments, Informed Consent Form (ICF) documents detailing study delivery data management activities, etc