Global Study Associate

AstraZeneca; Barcelona; On-site; EUR 48,000 - 72,000; Full time

Job summary

AstraZeneca is seeking a Global Study Associate to support the global study team in delivering clinical studies on time, within budget and to quality. You will assist with study setup, maintenance, and close‑out, coordinate regulatory documents, eTMF activities and cross‑functional tasks in compliance with ICH‑GCP and AZ SOPs.

Ideal candidates will have medical or biological science education, strong organizational skills, fluency in English, and the ability to train others and work

Qualifications

• Education in medical or biological sciences or discipline associated with clinical research preferred
• Proven organizational and analytical skills
• Previous administrative training/experience
• Computer proficiency in day‑to‑day tasks
• Develop working knowledge of the Clinical Study Process and ICH/GCP guidelines
• Excellent verbal and written communication in English
• Demonstrate ability to work independently, as well as in a team environment
• Ability to prepare presentation materials
• Demonstrate professionalism and mutual respect
• Willingness and ability to train others on study administration procedures
• Display excellent organization and time management skills, attention to detail, and ability to multi‑task in a high‑volume environment with shifting priorities

Responsibilities

• Support GS(A)D and GSMs by completing delegated study work.
• Initiate and lead the set-up of the electronic Trial Master File (eTMF) and maintain/close it to ICH/GCP and AZ SOPs.
• Provide oversight for non‑complex, non‑critical path vendors.
• Interact with internal staff and external stakeholders to collect regulatory documents.
• Contribute to regulatory submissions in information management systems and prepare CSR appendices.
• Create and maintain study documents with template and version control.
• Set up and maintain AstraZeneca tracking/communication tools.
• Support Clinical Trial Transparency activity in PharmaCM.
• Assist GS(A)D with tracking and payments in relevant systems.
• Coordinate study materials, equipment, and study close‑out logistics.
• Coordinate internal/external meetings and prepare materials for distribution.

Job description

The Global Study Associate is a member of the global study team supporting delivery of clinical studies within BioPharmaceuticals Clinical Operations, Study Management to time, cost and quality.

The GSA supports delivery of global clinical studies from study set-up through maintenance, close-out and study archiving. The GSA supports the Global Study Director (GSD), Global Study Associate Director (GSAD) and/or Global Study Manager (GSM) with coordinating activities, ensuring quality and consistency. The GSA supports with administration & systems and with other delegated aspects of clinical study execution in accordance with applicable clinical trial regulations (ex. ICH‑GCP), AstraZeneca (AZ) Standard Operating Procedures (SOPs), AZ policies & best practices and AZ values & behaviours.

Typical Accountabilities

• Support GS(A)D and GSMs by completing delegated study work. May work across many different studies and delivery models concurrently.
• Initiate and lead the set-up of the electronic Trial Master File (eTMF). Maintain and close the eTMF to ensure compliance to International Conference of Harmonisation Guidelines for Good Clinical Practice (ICH/GCP) and AZ SOPs.
• Provide oversight for non‑complex, non‑critical path vendors, ensuring compliance with study requirements and established processes.
• Interact/collaborate with internal staff and external stakeholders in collection of regulatory and other essential documents.
• Contribute to electronic applications/submissions in regulatory information management system by creating and managing clinical regulatory documents according to the requested technical standards and supporting effective publishing and delivery to regulatory authorities. Proactively plan and collate the administrative appendices for the CSR.
• Initiate, maintain and/or support the creation of study documents, ensuring template and version compliance per study specific requirements.
• Set‑up, populate and accurately maintain information in AstraZeneca tracking and communication tools and support team members in the usage of these tools.
• Support the set‑up, maintenance and close‑out of Clinical Trial Transparency (CTT) activity in PharmaCM, coordinating with relevant stakeholders to fulfil AstraZeneca compliance and meet the regulatory authority needs.
• Support the GS(A)D with tracking, reconciliation and follow-up of the study budget/payments in relevant systems, including the creation and maintenance of purchase orders, running invoice and payment reports.
• Contribute to application, coordination, supply and tracking of study materials and equipment.
• Contribute to collection of study supplies, if required, at the study close‑out.
• Coordinate and provide oversight of administrative tasks and logistical support throughout the conduct of the study, audits and regulatory inspections, according to company policies and SOPs.
• Lead the coordination and contribute to the preparation of internal and external meetings e.g., study team meetings, committee meetings, monitor meetings, Investigator meetings and virtual meetings. Liaise with internal and external participants and/or vendors.
• Prepare, contribute and distribute presentation material for meetings, newsletters and websites.
• Work on non‑drug project work in process improvements and/or leading improvement projects as discussed and agreed upon with their manager.
• Other duties as assigned and within scope of role.

Education, Qualifications, Skills and Experience

Essential

• Education in medical or biological sciences or discipline associated with clinical research preferred
• Proven organizational and analytical skills
• Previous administrative training/experience
• Computer proficiency in day‑to‑day tasks
• Develop working knowledge of the Clinical Study Process and an understanding of the range of working procedures relating to it, together with an understanding of the ICH/GCP guidelines.
• Excellent verbal and written communication in English
• Demonstrate ability to work independently, as well as in a team environment
• Ability to prepare presentation materials
• Demonstrate professionalism and mutual respect
• Willingness and ability to train others on study administration procedures
• Display excellent organization and time management skills, excellent attention to detail, and ability to multi‑task in a high‑volume environment with shifting priorities

Desirable

• Bachelor level education (or higher)
• Proven study admin/assistant or relevant experience on a study level
• Experience in clinical study lifecycle

Date Posted

20-oct-2026

Closing Date

30-oct-2026

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.