Senior Global Study Manager

At AstraZeneca we pride ourselves on crafting a collaborative culture that champions knowledgesharing ambitious thinking and innovation ultimately providing employees with the opportunity to work across teams functions and even the globe.

Recognizing the importance of individualized flexibility our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging facetoface in our offices 3 days a week. Our head office and BlueSky Hub in downtown Toronto are purposely designed with collaboration in mind providing space where teams can come together to strategize brainstorm and connect on key projects.

Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people the planet and our business are interconnected which is why were taking ambitious action to tackle some of the biggest challenges of our time from climate change to access to healthcare and disease prevention.

Introduction to role:

Are you ready to lead the operational activities that support and enable the delivery of clinical studies As a Senior Global Study Manager you will ensure quality and compliance in our clinical programs. Flexibility is key as accountabilities will vary depending on the nature of each clinical program.

Accountabilities:

• Provide operational expertise to the study team.
• Lead the development and updates of study documents ensuring template and version compliance.
• Prepare countryspecific agreements confidentiality agreements clinical trial applications and other applicable country documents.
• Foster team culture and promote team spirit within the GSMs and GSAs assigned to the study team.
• Mentor and guide the operations team to ensure effective collaboration and communication with the study team.
• Manage the setup of thirdparty vendors assess initial statements of work and budgets and handle the change order process.
• Provide input to data management documents and interface with data management representatives and sites to facilitate study data delivery.
• Initiate contract/budget requests track ongoing status facilitate generation of 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 as appropriate.
• Oversee thirdparty vendors global/local internal staff and investigator sites to support effective delivery of a study and its regulatory documents from protocol development through to the Clinical Study Report.
• Provide oversight of recruitment and data delivery as well as risk mitigation strategies.
• Oversee the clinical trial insurance process; track approvals revisions and renewals of certificates.
• Monitor study conduct and progress proactively identifying and resolving issues that may impact delivery of the study to the necessary quality timelines or budget.
• Drive risk management and quality efforts to ensure study compliance.
• Manage setup maintenance closeout and archiving of the Trial Master File (TMF) ensuring continual inspection readiness.
• Prepare presentation material for meetings newsletters and websites.
• Direct the study team in implementing audits and regulatory inspections.
• Identify areas of best practice/process improvements and share knowledge across the group.
• Contribute to the review of new/amended/unique SOPs and guidance documents.

Essential Skills/Experience:

• University degree/Bachelors degree preferably in medical or biological science or discipline associated with Clinical Research or equivalent experience
• Deep understanding of the drug development process with a minimum of 5 years clinical trial experience including at least 2 years in global study management
• Experience working with and delivering through strategic partners and 3rd party vendors
• Excellent knowledge of ICHGCP principles
• Teamoriented
• Ability to lead coordinate and prioritize multiple tasks and deliverables
• Proactive approach
• High degree of flexibility
• Demonstrated verbal and written communication skills
• Good negotiation and collaboration skills
• Demonstrated interpersonal and problemsolving skills
• Ability to manage change and actively seek and champion more efficient and effective ways of working
• Ability to coach & act as a buddy for more junior colleagues
• Some travel may be required

Desirable Skills/Experience:

• Early phase oncology clinical trial experience

Great People want to Work with us! Find out why:

• GTAA Top Employer Award for 11 years
• Top 100 Employers Award
• Canadas Most Admired Corporate Culture
• Learn more about working with us in Canada
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Are you interested in working at AZ apply today!

AstraZeneca 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.

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Date Posted