Global Study Associate Role at AstraZeneca USAÂ
The Global Study Associate job at AstraZeneca in Durham, North Carolina is a promising opportunity for professionals seeking clinical research jobs with global exposure. This associate job supports end-to-end clinical study activities while ensuring quality, compliance, and timely delivery in a collaborative work environment.
Job Details:
- Job Role: Global Study Associate
- Location: Durham, North Carolina, United States
- Job ID: R-242277
- Employment Type: Full-time
- Work Model: Hybrid (3 days onsite per week)
- Industry: Clinical Research / Life Sciences
About AstraZeneca:
AstraZeneca is a global, science-led biopharmaceutical company focused on the discovery, development, and commercialization of prescription medicines. Known for its strong commitment to innovation, sustainability, and patient-centric research, AstraZeneca fosters a collaborative culture that supports knowledge-sharing, global teamwork, and long-term career growth. The company actively addresses global health challenges, climate change, and access to healthcare through responsible science and innovation. Apply for more clinical research jobs in the USA.
Educational Requirements:Â
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Bachelor’s degree required
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Medical, biological sciences, or clinical research-related background preferred
Key Responsibilities for Global Study Associate role:
- Support global clinical studies from set-up to close-out and archiving
- Manage and maintain eTMF to ensure inspection readiness
- Coordinate delegated study activities across multiple studies
- Collect and manage essential and regulatory documents
- Support Clinical Trial Transparency and regulatory submissions
- Assist in vendor coordination, budget tracking, and invoice processing
- Prepare study documentation and support CSR planning
- Coordinate study materials, equipment, and close-out activities
Skills Required for Global Study Associate role:Â
- Strong organizational and time management skills
- High attention to detail and documentation accuracy
- Understanding of clinical study processes and ICH-GCP
- Proficiency with standard business tools and systems
- Clear written and verbal communication skills
- Ability to work independently and within cross-functional teams
Benefits of the Role:
- Exposure to global clinical studies and delivery models
- Career growth in clinical operations and research
- Flexible and hybrid working environment
- Collaborative and inclusive workplace culture
- Opportunity to contribute to impactful healthcare research
