Global Development Director Scientist

Posted date Sep. 08, 2026
Contract type Full time
Job ID R\-259665

Why choose AstraZeneca Spain?
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AstraZeneca Spain is a rising force in our global business. With headquarters in Madrid and our global hub in Barcelona, we’ve become an important international centre of excellence in the fight against critical disease. Boasting vibrant universities and business schools, the Barcelona ecosystem is a place where scientists can thrive. We attract a diverse workforce from across the globe, shining a beacon for innovation in a country that’s committed to clinical development.

We invite you to bring your talents to Barcelona where our respiratory medicine R\&D and Global Marketing centre offers opportunities in R\&D, IT, Commercial and HR. Or join us in Madrid and shape our growth in our BUs (Respiratory, Oncology \& CVRM ), and a range of Corporate functions. Additionally, you can find sales roles throughout the country. Together, we’re contributing to a world\-leading pipeline of therapeutics and delivering life\-changing medicines to patients.

Who do we look for?
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Calling all tech innovators, ownership takers, challenge seekers and proactive collaborators. At AstraZeneca Spain, breakthroughs born in the lab become transformative medicine for the world's most complex diseases. Alongside technical expertise, colleagues have the resilience, energy and collaborative mindset to change lanes, work with different teams and start projects from scratch.

Here, diverse minds and bold disruptors can meaningfully impact the future of healthcare using cutting\-edge technology. Whether you join us in Madrid or Barcelona, you can make a tangible impact within a global biopharmaceutical company that invests in your future. Join a talented global team that's powering AstraZeneca to better serve patients every day.

Success Profile
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Ready to make an impact in your career? If you're passionate, growth\-orientated and a true team player, we'll help you succeed. Here are some of the skills and capabilities we look for.

Diverse collaborators

This is a speak\-up culture that values collaboration. You’ll proactively bring your unique perspectives, experiences and skills to the table and seek the same from others. With our international team composition and the need for fast\-paced collaboration, you’ll always be building new connections with colleagues.

Cutting\-edge innovators

When you join us, you’ll be part of a team that embraces digital technology and data to transform the way we work and the work we do. Every day, you’ll help make history, empowered to ignite your creativity and build something enduring.

Resilient trailblazers

Here, the answers aren’t always available. So, you’ll need to bring a fearless, self\-starter mindset to navigate uncharted territories. You’ll harness your ceaseless energy to discover and make the necessary connections with colleagues to shape the future and achieve maximum impact.

Agile movers

Seize ownership and excel with autonomy to enjoy the constant rush of ground\-breaking discovery. Your ability to anticipate sudden shifts and adapt swiftly will prove critical as you make your mark in an environment that rewards initiative and resilience.

Responsibilities
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Job ID R\-259665 Date posted 09/08/2026
Location: Barcelona \- Spain (3 days working from the office and 2 days working from home)

About AstraZeneca

AstraZeneca is a global, science\-led, patient\-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. We are more than one of the world’s leading pharmaceutical companies.

AstraZeneca has a multifaceted environment that cultivates collaboration and innovation. We attract top minds, and we nurture and build talent.

Hematology Research and Development, Early and Late Development Hematology

Within Hematology R\&D, we are committed to advancing the science to deliver life\-changing medicines to patients most in need. With a combination\-focused pipeline that exploits the power of six scientific platforms (Immuno\-Oncology, Tumor Drivers and Resistance, DNA Damage Response, Antibody\-drug Conjugates, Cell Therapy and Epigenetics) to help address unmet clinical needs in a host of hematological cancers, we are motivated by a dedication to the scientific discovery and collaboration that will one day help eliminate cancer as a cause of death. This unit has responsibility for the value chain from discovery through to late\-stage development, enabling rapid acceleration of promising early\-stage assets and life\-cycle management programs

Role and Responsibilities

The Global Development Scientist Director is an important part of the Clinical Project Team (CPT), and Global Study Team (GST) working harmoniously and cross functionally (in a matrix environment) with other CPT \& GST members, Site Management \& Monitoring (SMM), field\-based liaisons, and site personnel. The Global Development Scientist Director and counterpart Global Development Medical Director work collaboratively in the clinical aspects underpinning a product.

This includes shared responsibility with Clinical Operations team members in the planning and execution, including recruitment and delivery of a clinical study. Accountabilities include clinical support for the development and implementation of early and/or late phase AstraZeneca sponsored clinical program strategies. As such, you will provide scientific input into design \& implementation of clinical trial(s), their delivery, clinical data review and data cleaning, interpretation of results, reporting successfully on time, and activities required for worldwide registration of the product (i.e. clinical input to NDA/BLA).

The Global Development Scientist Director may also provide expert input or lead functional process improvement initiatives and provide contributions to cross\-asset or cross\-tumor area working groups depending on the level of experience.

This position demands strong collaborative communication skills, including the ability to engage with and influence a diverse range of stakeholders both within and external to AstraZeneca. The individual will operate according to the highest ethical standards in compliance with internal SOPs, local regulations, laws and adhere to Good Clinical Practice (GCP) and regulatory requirements.

Main duties:

• Work cross functionally within CPT to ensure the clinical strategy is translated into the development of the study concept document, study protocol and related documents


• Provide clinical/scientific input into design \& implementation of clinical trial(s), including studies involving immunotherapy and cell therapy approaches, their delivery, clinical data review and data cleaning, interpretation of results, reporting successfully on time, and activities required for worldwide registration of the product (i.e. clinical input to NDA/BLA).


• Establish key relationships internally with clinical project teams, and externally with regulatory bodies and external service providers.


• Accountable for the relevance and accuracy of clinical science underpinning of clinical study based on detailed scientific review and consultation, for the clinical and scientific leadership and integrity of protocols and/or components of clinical plans and for the delivery of final protocol and its governance approval.


• Lead the development of the protocol and related documents and the development and delivery of the clinical study report to meet GCP, ICH and all AstraZeneca quality standards.


• Lead cross functional projects to ensure the successful passage of drugs through all phases of the drug development process, or contribute to one or more elements of such a project as a technical expert.


• Review and interpret medical data and clinical trial data and come up with conclusions with Medical Director


• You will support the development of clinical components of regulatory and EC/IRB submission documents for instances where marketing approval is warranted. Prepare and provide input to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, PSUR, regulatory responses)


• Participate or lead as needed the review and assessment of new opportunities and ESRs.


• Responsible for timely responses to investigational study sites for local ICF changes, protocol \& EC/IRB questions/requests.


• Contribute to development and delivery of face to face or virtual investigator and supervise training.

• BS required, PhD in a scientific field, PharmD or MD is strongly preferred


• Minimum of 5 years of relevant experience


• Industry or Academic experience in drug development required with experience in malignant haematology clinical trials strongly preferred.


• Sufficient technical knowledge (haemato\-oncology background preferred) to be able to interact with confidence with internal and external partner


• Possesses sound foundational knowledge of FDA and other major country regulations and detailed knowledge of Good Clinical Practice other regulations governing clinical research.


• Possesses general knowledge of 1\) medical monitoring 2\) Regulatory approval process in relevant countries; 3\) pharmaceutical industry/R\&D operations; 4\) marketing and commercial fundamentals.


• Drug Development/Clinical Development Planning: Demonstrates a consistent track record to both independently complete, and lead peers in completion in components of sophisticated plans, related documents, appropriate methodologies, measures, analytical plans and evaluation tools.


• Ability to drive/contribute to protocol design, writing and implementation.

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