.Join our dynamic team as a Global Study Associate, a key player in the extended global study team supporting the delivery of clinical studies within BioPharmaceuticals Clinical Operations, Study Management. This role is integral to ensuring our studies are delivered on time, within budget, and to the highest quality. As a GSA, you will support the Global Study Director (GSD), Global Study Associate Director (GSAD) and/or Global Study Manager (GSM) with coordinating activities, ensuring quality and consistency. Your role will involve administration & systems support and other delegated aspects of clinical study execution in accordance with applicable clinical trial regulations (ex. ICH-GCP), AstraZeneca (AZ) Standard Operating Procedures (SOPs), AZ policies & best practices and AZ values & behaviours.Accountabilities:Support GS(A)D and GSMs by completing delegated study work.Initiate and lead the set-up of the electronic Trial Master File (eTMF).Maintain and close the eTMF to ensure compliance to International Conference of Harmonisation Guidelines for Good Clinical Practice (ICH/GCP) and AZ SOPs.Interact/collaborate with internal staff and external stakeholders in collection of regulatory and other essential documents.Contribute to electronic applications/submissions in ANGEL by creating and managing clinical regulatory documents according to the requested technical standards.Essential Skills/Experience:Education in medical or biological sciences or discipline associated with clinical research preferred.Proven organizational and analytical skills.Previous administrative training/experience.Computer proficiency in day-to-day tasks.Develop working knowledge of the Clinical Study Process and an understanding of the range of working procedures relating to it, together with an understanding of the ICH/GCP guidelines.Excellent verbal and written communication in English.Demonstrate ability to work independently, as well as in a team environment.Ability to prepare presentation materials.Demonstrate professionalism and mutual respect.Willingness and ability to train others on study administration procedures.Display excellent organization and time management skills, excellent attention to detail, and ability to multi-task in a high-volume environment with shifting priorities.Desirable Skills/Experience:Bachelor level education (or higher).Proven study admin/assistant or relevant experience on a study level.Experience in clinical study lifecycle.When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world
