Global Study Associate Manager

AstraZeneca • Mississauga, ON

2d • CA$81,685 - CA$107,211 • Hybrid

About The Position

As a Global Study Associate Manager (GSAM) at AstraZeneca, you'll be at the heart of delivering clinical studies from inception to completion. This dynamic role involves collaborating with internal and external partners to ensure the successful execution of clinical studies across various therapeutic areas and phases. You'll lead administrative activities, oversee compliance tracking systems, and support vendor oversight, all while contributing to the development of Clinical Study Reports and study archiving. Join us in pushing the boundaries of science and making a difference in patients' lives!

Requirements

• Bachelor’s degree or equivalent in clinical practice/health care, life sciences, or drug development, or commensurate work experience.
• Proficiency with technological systems (Microsoft Office such as: Excel, PowerPoint, and SharePoint Online, eTMF and Veeva Systems).
• Excellent organizational communication and time management skills.
• Highly proactive and willing to take initiative.
• Strong relationship building skills.
• As is typical of an office-based role, employees must be able, with or without an accommodation to: use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.

Nice To Haves

• Over 3 years supporting global study teams in a clinical research environment.
• Ability to drive discussions around the scope of work and oversee vendor-related activities.
• Excellent knowledge of Essential Documents, CFR, and/or ICH-GCP.
• Demonstrated ability to collaborate as well as work independently.
• Project management skills and basic PM methodology.

Responsibilities

• Collaborate with global study teams and key vendors to support clinical study execution, ensuring adherence to timelines and quality standards.
• Lead the preparation of study documents and vendor-related documents, such as the Vendor Oversight Plan.
• Facilitate interactions with cross-functional team members, including Data Management, Procurement, Regulatory, Patient Safety, and Quality Assurance.
• Execute delegated aspects of the clinical study in alignment with objectives set by the GPD, GSAD, or GSM.
• Contribute to the planning and execution of both internal and external meetings.
• Identify risks and issues proactively, developing mitigation and action plans.
• Support project and budget management for the GSM, adhering to agreed-upon delegation.
• Participate in or lead departmental initiatives and/or Subject Matter Expert (SME) functions.
• Mentor team members, promoting professional development and a collaborative work environment.
• Provide support for other study and functional activities as assigned.

Benefits

• Annual base salary for this position ranges from 81,684.80 to 107,211.30.
• Annual Variable Pay Bonus/Short Term Incentive opportunity
• Eligibility to participate in our equity-based long-term incentive program (if applicable to role).
• Competitive Flex Benefits & Retirement Savings Program
• 4 weeks’ paid vacation
• annual Personal Days.
• Contract Benefits Program

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level