Global Study Manager, Oncology R&D, Early Oncology Clinical

Global Study Manager, Oncology R&D, Early Oncology Clinical - SecondmentJoin to apply for the Global Study Manager, Oncology R&D, Early Oncology Clinical - Secondment role at AstraZenecaIntroduction To Role Are you ready to make a difference in the world of clinical research? As a Global Study Manager, you'll play a pivotal role in supporting the delivery of clinical studies with a focus on quality and compliance. This dynamic position requires flexibility as you navigate the unique challenges of each clinical program.AccountabilitiesContribute to the development and updates of study documents, ensuring template and version compliance.Lead the preparation of country-specific agreements, confidentiality agreements, clinical trial applications, and other applicable country documents.Manage the setup of third-party vendors, assessing initial statements of work and budgets, and overseeing the change order process.Provide input to data management documents and collaborate with data management representatives and sites to facilitate study data delivery.Initiate contract/budget requests, track ongoing status, facilitate purchase orders, review vendor invoices, and assist in tracking spend against approved budget.Ensure the supply of investigational products and study materials by liaising with Drug Supply or external service providers.Oversee third-party vendors, global/local internal staff, and investigator sites to support effective study delivery from protocol development to Clinical Study Report.Provide oversight and support for recruitment, data delivery, and risk mitigation strategies.Assist in the clinical trial insurance process; track approvals, revisions, and renewals of certificates.Monitor study conduct and progress, proactively identifying and resolving issues impacting study delivery.Support risk management and quality efforts to ensure study compliance.Support setup, maintenance, closeout, and archiving of the Trial Master File (TMF), ensuring continual inspection readiness.Prepare presentation material for meetings, newsletters, and websites.Support the study team in implementing audits and regulatory inspections.Contribute to the review of new/amended/unique SOPs and guidance documents.Essential Skills/ExperienceUniversity degree/Bachelor’s degree in medical or biological science or discipline associated with Clinical Research, or equivalent experienceMinimum of 3-4 years of progressive clinical trial experienceUnited States only: Bachelor's Degree and 3+ years of experience, Associate's degree plus 7+ years of experience or High School plus 11+ years of experienceExperience working with and delivering through strategic partners and 3rd party vendorsExcellent knowledge of ICH-GCP principlesTeam-orientedAbility to coordinate and prioritize multiple tasks and deliverablesProactive approachHigh degree of flexibilityDemonstrated verbal and written communication skillsGood negotiation and collaboration skillsDemonstrated interpersonal and problem-solving skillsSome travel may be requiredDesirable Skills/ExperienceEarly phase oncology clinical trial experienceGlobal study management experienceGreat People want to Work with us Find out why:GTAA Top Employer Award for 10 yearsTop 100 Employers AwardCanada’s Most Admired Corporate CultureLearn more about working with us in CanadaView our YouTube channelAstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing AZCHumanResources@astrazeneca.com.Date Posted 10-Nov-2025Closing Date 16-Nov-2025 #J-18808-Ljbffr