Global Study Manager - Mississauga, Canada - AstraZeneca

AstraZeneca

Verified Company

Mississauga, Canada

1 week ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Location:
Mississauga office (Hybrid 3 days in 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 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 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.

Our Oncology Research and Development Team:
Oncology is driven by speed. Here you will be backed by leadership and empowered at every level to prioritize and make bold moves.

Our pioneering approach is identifying and treating patients earlier, focusing on early stage cancer trials and listening and evolving based on their needs.

Join a dedicated Oncology team that's growing fast and building a strong track record of success.

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 crossfunctionally 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 Leader (GSL) 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 GSL with budget management, such as external service provider invoice reconciliation
You make sure studies are inspectionready at all times according to ICH-GCP, AZ SOP and relevant policies/guidelines
You will ensure that all study documents in scope of GSAM'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 GSL
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 nondrug 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

AstraZeneca is committed to taking every reasonable precaution to protect employees, our customers and the healthcare systems in the communities in which we serve.

In an effort to protect the wellbeing of our employees and customers, full COVID-19 vaccination is an essential requirement of all positions at AstraZeneca.

As such, all offers of employment will be conditional upon either (i) proof of full COVID-19 vaccination or (ii) proof of need for accommod