• Job Description

  Req#: R-175887

  Global Study Manager

  12 Month Contract with possibility of extension depending on performance and business needs

  Hybrid Work- 3 days/week from our Mississauga, ON 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 GSM’s 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

  Essentials for the role:

  • 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

  • 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

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

  • GTAA Top Employer Award for 9 years

  • Learn about our culture

  • Learn more about working with us in Canada

  • View our YouTube channel

  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 .

  Date Posted

  19-Oct-2023

  Closing Date

  02-Nov-2023

  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.

• About the company

  AstraZeneca PLC is a British-Swedish multinational pharmaceutical and biopharmaceutical company with its global headquarters in Cambridge, England.

Notice