Global Study Associate at AstraZeneca

Durham, North Carolina, United States -

Full Time

Start Date

Immediate

Expiry Date

21 Mar, 26

Salary

0.0

Posted On

21 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Organization, Time Management, Attention To Detail, Communication, Clinical Study Processes, Regulatory Compliance, Vendor Management, Budget Tracking, Collaboration, Presentation Skills, Proactivity, Professionalism, Respectfulness, Independence, Teamwork, Learning

Industry

Pharmaceutical Manufacturing

Description

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 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. Be the engine behind high-quality clinical study delivery. As a Global Study Associate (GSA), you’ll support global studies end-to-end—set-up, maintenance, close-out, and archiving—so we deliver to time, cost, and quality while upholding ICH-GCP, AZ SOPs, and our values. You’ll partner closely with the GSD, GSAD, and GSM to coordinate activities, drive consistency, and keep our studies moving. What you’ll do Own study essentials: Set up, maintain, and close the eTMF; ensure documentation is compliant and inspection-ready. Coordinate operations: Support delegated study tasks across multiple studies; manage trackers, systems, communications, and logistics. Enable compliance: Collect and manage regulatory/essential documents; support submissions and Clinical Trial Transparency activities. Manage vendors and budgets: Oversee non-complex vendors and help track budgets, POs, invoices, and payments. Create clarity: Prepare and maintain study documents and administrative appendices; support CSR planning and delivery. Support supply readiness: Coordinate study materials/equipment and support close-out activities. What you’ll bring Education: Bachelor’s degree (medical/biological sciences or clinical research-related preferred). Experience: Study admin/coordination experience across the clinical study lifecycle. Skills: Strong organisation, time management, and attention to detail; confident with standard business tools and systems. Knowledge: Working understanding of clinical study processes and ICH-GCP; ability to learn AZ procedures quickly. Communication: Clear written and verbal English; able to prepare presentations and collaborate across teams and with external partners. Ways of working: Proactive, professional, and respectful; comfortable working independently and in teams; willing to train others. Why this role matters Impact: Your precision and coordination keep our studies inspection-ready and on schedule. Growth: Exposure to global studies, diverse delivery models, and cross-functional partners—ideal for a clinical operations career. 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. #LI-Hybrid Date Posted 20-Dec-2025 Closing Date 04-Jan-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form. AstraZeneca is a global, science-led, patient-focused biopharmaceutical company. We focus on discovering, developing and commercialising prescription medicines for some of the world’s most serious diseases. But we are more than one of the world’s leading pharmaceutical companies. At AstraZeneca, we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science, challenge convention and unleash your entrepreneurial spirit. To embrace differences and take bold actions to drive the change needed to meet global healthcare and sustainability challenges. There is no better place to make a difference in medicine, patients, and society. An inclusive culture where you will connect different thinking to generate new and valuable opportunities. Where you will find a commitment to lifelong learning, growth and development for all. Our Inclusion & Diversity (I&D) mission is to create an inclusive and equitable environment where people belong, using the power of our diversity to push the boundaries of science to deliver life-changing medicines to patients. Inclusion and diversity are fundamental to the success of our company, because innovation requires breakthrough ideas that only come from a diverse workforce empowered to challenge conventional thinking. We’re curious about science and the advancement of knowledge. We find creative ways to approach new challenges. We’re driven to make the right choices and be accountable for our actions. As an organisation centred around what makes us human, we put a big focus on people. Across our business, we want colleagues to wake up excited about their day at the office, in the field, or in the lab. Along with our purpose to bring life-changing medicines to people across the globe, we have a promise to you: to help you realise the full breadth of your potential. Here, you’ll do work that has the potential to change your life and improve countless others. And, together with your team, you’ll shape a culture that unites and inspires us every day. This is your life at AstraZeneca.

Responsibilities

The Global Study Associate will support global studies end-to-end, including set-up, maintenance, close-out, and archiving. They will coordinate activities, drive consistency, and ensure compliance with regulations and documentation.