# Local Study Associate Director at AstraZeneca

AstraZeneca is hiring a Local Study Associate Director. Level rates it Little AI ●○○○; you can [apply on AstraZeneca](https://jobsbylevel.com/go/a2fbaa0c-dc15-459a-a2b2-6fbd51dc48d8?utm_medium=ai-agent).

AI Level 1, AI centrality 38 out of 100. Taiwan.

## Details

- Company: [AstraZeneca](https://jobsbylevel.com/companies/astrazeneca)
- AI level: AI Level 1 (score 38 out of 100)
- Location: Taiwan
- Posted: October 28, 2026
- Apply: https://jobsbylevel.com/go/a2fbaa0c-dc15-459a-a2b2-6fbd51dc48d8?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=local-study-associate-director-at-astrazeneca-19e325

## Description

Typical Accountabilities - Coordinate lifecycle management, enhancement, and business continuity for Study Delivery processes, systems, reporting, and technology across the clinical research portfolio. - Develop, implement, and continuously improves reporting tools, metrics, and analytical processes, identifying new opportunities for optimization and efficiency. - Lead the delivery of centrally managed study services—such as document management, clinical trial transparency, and system training—to ensure consistency, compliance, and best practice across all drug projects. - Serve as the principal contact for document management activities from initial production/import through completion of the Clinical Study Report and regulatory archiving. - Collaborate with internal stakeholders (Study Delivery, Clinical Development, Data Management, Patient Safety, Compliance) and external partners (service providers, regulatory bodies) to ensure seamless study administration and regulatory compliance. - Facilitate dynamic communication channels to share knowledge, disseminate best practices, and provide guidance and training on current and evolving study systems, standards, and procedures. - Act as a subject matter expert for risk management, contingency planning, and change management, proactively identifying and resolving operational issues or process non-compliance. - Maintain up-to-date awareness of external trends, regulatory requirements, and enabling technologies in clinical trial management to drive the adoption of fit-for-purpose solutions and business process improvements. - Manage and track study materials, equipment, and controlled documents to ensure high standards of quality and audit readiness. - Oversee administrative tasks (including audit and inspection support), ensuring robust documentation practices and regulatory compliance throughout all phases of study execution. - Advise and support project teams in developing and implementing effective study methodologies, harmonized processes, and regulatory best practices. Qualifications and Skills Essential: Bachelors of Science degree in related discipline, preferably in medical or biological science, or equivalent work experience in directly related fields of endeavors; Significant experience in the pharmaceutical industry working in an environment of clinical study delivery/clinical development processes; Demonstrated aptitude for process and technology; Experience with process and training design and implementation; Demonstrated leadership ability in a team environment; proven ability to facilitate team building and teamwork; Proven leadership experiences (people and project) including team facilitation skills and strong collaborative communications ability to diverse client base; Excellent written and verbal communication skills in English; Proven excellent negotiation, collaboration, interpersonal, problem solving and conflict resolution skills; Proven Project Management skills; Experience working internationally; Ability to travel both domestic and international; Customer focused; Performance driven. Desirable: Advanced degree in biological sciences, healthcare related field or business; Clinical study delivery operational experience; Experience in cross-functional pharmaceutical development; In depth understanding of Business Continuity Planning.; Ability to effectively lead complex non-drug projects in a world-wide environment through in depth understanding of AZ PMF, IPOM and DMAIC Change Management processes; Demonstrated ability to set and manage priorities, resources, performance targets and project initiatives in a global and regional environment; Proven Conceptual, Analytical and Strategic thinking; concern for standards and willingness to learn from others; Proven Project management skills; Demonstrates operational expertise in risk management and contingency planning; Has in depth knowledge of GCP, AZ Procedural documents, as they pertain to Study delivery

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/local-study-associate-director-at-astrazeneca-19e325

Source: https://jobsbylevel.com/jobs/local-study-associate-director-at-astrazeneca-19e325

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