Global Study Manager, Haematology (12 Month Contract)
Global Study Manager, Haematology
Hybrid Work- 3 days/week from Mississauga office
At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, 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 face-to-face in our offices 3 days a week. Our head office is 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 we’re taking ambitious action to tackle some of the biggest challenges of our time, from climate change to access to healthcare and disease prevention.
What you’ll do:
You are a member of the extended global study team supporting delivery of clinical studies to time, cost and quality from Clinical Study Protocol (CSP) development through to study archiving.
You will work cross-functionally building partnerships with internal and external partners to deliver and provide oversight to ensure successful study delivery
You will maintain and facilitate interactions with internal functions including Data Management, Procurement, Regulatory, Patient Safety and Quality Assurance, and external functions including the CROs and other outside service providers to ensure an efficient study delivery.
You will lead and/or participate in the preparation of delegated study documents (e.g. Informed Consent Form, master Clinical Study Agreement etc.) and external service provider related documents (e.g. specifications)
You will support the Global Study Associate Director (GSAD) in project management as per agreed delegation
You ensure the supply of study materials and Investigational product by liaising with Clinical Supply Chain or external service providers
You help support the GSAD with budget management, such as external service provider invoice reconciliation
You make sure studies are inspection-ready at all times according to ICH-GCP, AZ SOP and relevant policies/guidelines
You will ensure that all study documents in scope of Global Study Manager's (GSM) responsibilities are completed and verified for quality in the Trial Master File
You will assist with the planning and conduct of internal and external meetings (e.g. Investigator/Monitors meeting)
You will monitor study conduct and progress, identifying and resolving risks and issues which may impact delivery of the study to the necessary quality, timeline or budget objectives with the GSAD
You will contribute to ad hoc team productivity and efficiency by providing direction and facilitating positive team dynamics
You will have the opportunity to provide input into non-drug project work including training activities and the development of procedures as needed
You are responsible for collecting and reporting Adverse Events in accordance with AstraZeneca policies and SOPs
Essential Qualifications/ Experience
University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research
Minimum 3 years experience within the pharmaceutical industry supporting clinical operations
Haematology/Oncology experience
Shown project management, organizational and analytical skills
Knowledge of clinical development / drug development process across various phases and therapy areas as well as relevant knowledge of international guidelines ICG-GCP
Computer proficiency
Excellent knowledge of spoken and written English
Desired Qualifications:
Global clinical research experience in managing multiple countries
Vendor management
Sponsor experience or having worked in a Functional Service Provider (FSP) model previously for another sponsor
Great People want to Work with us! Find out why:
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 AZCHumanResources@astrazeneca.com.
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
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