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Global Study Manager

On-site in Barcelona·Full-time·Added 3 days ago

AstraZeneca

40 open roles

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Overview

Job details

Full-time hours
Per the ad.

Requirements

Have the right to work in Spain
AstraZeneca doesn't mention sponsorship in the ad.
Work in English
English is required, per the ad.
Work on-site in Barcelona
No relocation package mentioned.
Have 3+ years of experience
Mid-level role.
University degree
“University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.” — per the ad.

Requirements

What we're looking for

· 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

Nice to have

· Advanced degree

· Experience in all phases of a clinical study lifecycle

· Basic knowledge of GXP outside of GCP (i.e GMP/GLP)

The role

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.

What you'll do

· 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 delivery to time, costs and quality objectives.

· Contributes to the planning and conduct of internal and external meetings (e.g., Investigators'/Monitors' meeting).

· Ensures the supply of Investigational product and study materials by liaising with Clinical Supply Chain or external service providers as appropriate.

· Proactively contributes to risk and issue identification, development of mitigation and/or action plans for identified risks and issues.

· Ensures that all study documents in scope of GSM's responsibilities are complete and verified for quality in Trial Master File.

· Supports GSD and/or GSAD with budget management, such as external service provider invoice reconciliation.

· Adheres to global clinical processes, procedural documents, applicable Quality & Compliance manual documents and international guidelines such as ICH/GCP to ensure study is inspection ready at all times.

· Supports GSD and/or GSAD with overall project management as per agreed delegation.

· For outsourced studies, supports GSD and/or GSAD in management of the CRO Project Manager to ensure study delivery according to agreed timelines, budget and quality standards, while ensuring that the appropriate level of oversight of the CRO is maintained and documented throughout the lifecycle of the study, in accordance with relevant AZ SOPs and guidelines (e.g., description of services and transfer of obligations)

· Take on assignments on non-drug project work in process improvements and/or leading improvement projects as discussed and agreed upon with their manager

Date/Closing Date

30-sept-2026

13-oct-2026

Hiring process

2 steps1 interviewa task to do

Application
Recruiter contact · With a recruiter
Assessment
Not every role
Some roles, especially graduate roles, add a game-based assessment, a video or telephone interview, or an assessment day.
Interview
A two-way conversation about your skills and suitability for the role, and a chance for you to find out if AstraZeneca is right for you.
Pre-employment screening
Offer

Candidates who reach interview stage or beyond usually get feedback within 14 days of the role's closing date.
Interview travel expenses are reimbursed for journeys over 100km.
Alcohol and drug testing is carried out for new hires where required by local country legislation.

About AstraZeneca

AstraZeneca is a global, science-led biopharmaceutical company that discovers, develops, and commercializes prescription medicines in therapeutic areas including oncology, cardiovascular, renal and metabolism, and respiratory and immunology. With a workforce of over 80,000 employees worldwide, the company is headquartered in Cambridge, UK, and operates across more than 100 countries, focusing on innovative medicines and advanced technologies like AI and data science to transform patient care.

In Spain, AstraZeneca has a significant presence with offices in Madrid and Barcelona, contributing to clinical development, regulatory affairs, and commercial operations. The company is known for its collaborative and inclusive culture, offering international professionals opportunities to work on global projects, particularly in areas like cell therapy, AI-driven health solutions (Evinova), and patient safety. With a strong commitment to diversity and innovation, AstraZeneca Spain is an attractive destination for talent seeking to make a global impact while living in Spain.

Industry: Pharma
Founded: 1999
Employees: 10,000+
Headquarters: Cambridge, UK
In Spain: Madrid, Barcelona
Website: astrazeneca.es

Good to know if you are moving

AstraZeneca offers a global, multicultural work environment with opportunities to collaborate with colleagues across the world.
The company has a strong commitment to employee development and offers various career growth programs.
Spain offices are located in major cities like Madrid and Barcelona, offering a high quality of life and vibrant culture.
AstraZeneca is a leader in innovative therapies, providing employees with the chance to work on cutting-edge medical advancements.
The company supports flexible working arrangements and promotes a healthy work-life balance.

In their own words

Additional information

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.

All open roles at AstraZeneca