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:As a Global Study Associate, you will be responsible for supporting GS(A)D and GSMs by completing delegated study work. You may work across many different studies and delivery models concurrently. Your tasks will include initiating and leading the set-up of the electronic Trial Master File (eTMF), maintaining and closing the eTMF to ensure compliance to International Conference of Harmonisation Guidelines for Good Clinical Practice (ICH/GCP) and AZ SOPs, interacting/collaborating with internal staff and external stakeholders in collection of regulatory and other essential documents, and much more. You will also contribute to electronic applications/submissions in ANGEL by creating and managing clinical regulatory documents according to the requested technical standards and supporting effective publishing and delivery to regulatory authorities.Education in medical or biological sciences or discipline associated with clinical research preferredProven organizational and analytical skillsPrevious administrative training/experienceComputer proficiency in day-to-day tasksDevelop 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 guidelinesExcellent verbal and written communication in EnglishDemonstrate ability to work independently, as well as in a team environmentAbility to prepare presentation materialsDemonstrate professionalism and mutual respectWillingness and ability to train others on study administration proceduresDisplay excellent organization and time management skills, excellent attention to detail, and ability to multi-task in a high-volume environment with shifting prioritiesBachelor level education (or higher)Proven study admin/assistant or relevant experience on a study levelExperience in clinical study lifecycleReady to embrace new and varied opportunities to develop and learn? Join us and be part of a team that makes a bigger impact on patients' lives. Apply now!#J-18808-Ljbffr
