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Global Study Associate (Contract)
Company | AstraZeneca |
Address | Mississauga, Ontario, Canada |
Employment type | FULL_TIME |
Salary | |
Category | Pharmaceutical Manufacturing |
Expires | 2023-08-12 |
Posted at | 10 months ago |
Global Study Associate (12 month contract)
- Handle the collection, reviewing, and tracking of relevant study documents in the TMF.
- Set-up, populate and accurately maintain information in AZ tracking and communication tools (e.g. CTMS, SharePoint, MS Teams etc.) and support team members in the usage of these tools.
- Contribute to and distribute meeting material and other varied forms of communication.
- Support the GSD, GSAD and/or GSM by completing delegated study work as required. May work across many different studies and delivery models concurrently.
- Interact/collaborate with internal and external partners in collection of regulatory and other documents/information.
- Set-up, maintain and close the Trial Master File (TMF) as delegated by the GSD/GSAD. Ensure compliance to ICH-GCP and AZ SOPs.
- Support production of study documents (as delegated), ensuring template and version compliance per study-specific requirements.
- Contribute to electronic applications/submissions in ANGEL by creating and managing clinical-regulatory documents according to the requested technical standards and supporting effective publishing and delivery to regulatory authorities. Collate the administrative appendices for the Clinical Study Report.
- Computer proficiency in day-to-day tasks
- Administrative knowledge and basic knowledge in drug development and ICH-GCP
- Demonstrate ability to work independently, as well as in a team environment
- Ability to prioritize appropriately and to be adaptable
- Organizational, time management & analytical skills; excellent attention to detail and ability to multi-task in a fast-paced and dynamic environment
- Excellent verbal and written communication in English
- Study administration experience
- Bachelor’s degree (or higher)
- Experience in supporting clinical trials and study development
- Experience within the pharmaceutical industry
- Education in medical or biological sciences or subject associated with clinical research
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