Study Delivery Associate Internship - Mississauga, Canada - AstraZeneca

AstraZeneca

Verified Company

Mississauga, Canada

2 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

InternshipSHIP

Description

Study Delivery Associate Internship (4 months, Fall Placement)
**Hybrid Work

3 days/week at our Mississauga, ON office**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 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 position

The Study Delivery Associate (SDA) is a key member of our clinical team responsible for managing clinical study trials for patients in Canada.

This role will interact with external clinical experts and our internal clinical colleagues to deliver quality clinical trials and provide support and feedback into day-to-day activities.

What you'll do

Approve sites for drug shipment
Prepare, execute, track, collect, review and assess clinical documents while ensuring their completeness according to regulatory guidelines
Assist external investigational site staff with the accurate and timely completion of ethics and regulatory documents in accordance with the regulatory and GCP guidelines
Review the study scope and design to provide input into the site level activation and risk mitigation plan and give ongoing study/site level problem solving throughout the study
Support the study lead, by reviewing and contributing to the development and preparation of all study/site level documents as required (for example: Study Management Agreements, delegation of responsibility, Clinical Study Agreements, etc.)
Support the study regulatory and ethics submission process
Ensure audit readiness, by conducting quality checks of SMF documents according to the study Quality Control Plan
Input and review payment terms and fee schedule of the Clinical Study Agreement.
Review, assess, approve and process payments associated with Agreements, to be in line with the terms of the agreement and financial guidelines
Set up and maintain payment terms within the appropriate systems.
Review, analyze and resolving payment discrepancies and queries
Lead nondrug supplies, by developing, inputting into, sourcing, ordering, initiating the shipment, tracking, reviewing stock level, and approving materials for destruction
Prepare and execute Statement of Work (SOW) with vendor for local drug management
Collaborate with Global Investigational Product Supplies units to ensure precise delivery of clinical drug supplies
Communicate with global study teams and local regulatory contacts, to assess Canadian requirements for comparator and/or rescue medication, and source from local providers if required

Essentials for the role:

Currently enrolled in the post graduate Clinical Research program and nearing graduation
Understanding of Good Clinical Practices/International Committee on Harmonization principles
Strong social and interpersonal skills (written and oral)
Ability to influence without authority
Ability to work effectively both independently and in a team environment
Selfmotivated and able to display autonomy and initiative
Strong attention to detail with exceptional project management skills
Effective time management skills
Passion for customer service
Good knowledge of MS Office (Word, Excel, PowerPoint) using multiple computer systems
Bilingualism in French would be considered an asset.

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