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Global Study ManagerAstraZeneca · Spain - Barcelona
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AstraZeneca

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Global Study Manager

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🗓️ Posted 2026-09-30 Spain - Barcelona Full-time Hybrid Healthcare Medical
💰 Salary Not shared 📊 Market 3,800 GBP–5,500 GBP/mo

About the Company

The Global Study Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations, Study Management to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving. The GSM works cross-functionally with internal and external partners to deliver delegated aspects of the clinical study in accordance with Global Study Director (GSD) or Global Study Associate Director (GSAD) in delegated aspects of clinical study execution in accordance with the Delivery Model, AZ Project Management Framework, current clinical trial regulations (e.g. ICH GCP), AstraZeneca Standard Operating Procedures (AZ SOPs), AZ policies and best practices (e.g. AZ guidelines) and in line with AZ values and behaviours. Typical Accountabilities In partnership with AZ team, other AZ clinical experts and external service providers, the GSM provides oversight to ensure study delivery. Leads/contributes to the preparation of delegated study documents (e.g., Informed Consent Form, master Clinical Study Agreement etc), and external service provider related documents (specifications, study specific procedures, descriptions, presentations etc.). Maintains and facilitates interactions with internal functions and external functions including the CROs and other external service providers to ensure an efficient study d

Requirements

  • ● University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.
  • ● Relevant experience from within the pharmaceutical industry or similar organization or academic experience, preferably of at least 3 years.
  • ● Knowledge of clinical development / drug development process in various phases of development and therapy areas
  • ● Excellent knowledge of international guidelines ICH/GCP
  • ● Excellent communication and relationship building skills, including external service provider management skills
  • ● Good project management skills
  • ● Demonstrated ability to collaborate as well as work independently
  • ● Demonstrated leadership skills
  • ● Computer proficiency, advanced computer skills in day-to-day tasks
  • ● Excellent verbal and written communication in English
  • ● Advanced degree
  • ● Experience in all phases of a clinical study lifecycle
  • ● Basic knowledge of GXP outside of GCP (i.e GMP/GLP)
  • ● Date Posted 30-sept-2026
  • ● Closing Date 13-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.