Why choose AstraZeneca Spain?

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?

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.

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.

Role Barcelona onsite 3 days office/2 days home

Would you like to be part of a fast-paced and agile global team that has direct strategic impact on drug development, empowered and trusted to innovate and experiment? Join us at AstraZeneca CVRM (Cardiovascular Renal Metabolism) Biometrics to impact a wide range of engaging projects striving to make a difference for millions of patients. Our Biometrics team consists of Statisticians, Statistical Programmers, Information and Data Scientists. We drive and contribute to optimized clinical drug development programs and access to information and scientific knowledge management.

We are now offering an exciting opportunity for a dedicated and highly motivated individual to join us as Statistical Programming Associate Director.

This role is a delivery focused technical leadership role for programming and overseeing deliverables with quality and timeliness, following established standards and processes. This leadership role requires profound programming experience and excellent industry knowledge to independently lead implementation of programming activities and guide other programmers. You will provide subject matter expertise within the Programming discipline and act as a specialist within cross-functional teams to deliver continuous improvement.

This role will be placed at AstraZeneca’s dynamic R&D global hub in Barcelona (Spain), where you will work in an international environment at the forefront of clinical development.

Accountabilities:

As a Statistical Programming Associate Director, you are responsible for leading and directing the full scope of project delivery and/or lead a technical project within the TA/Drug Project/Study/Function.

Typical accountabilities include:

• Leading implementation of statistical programming aspects of the protocol or clinical development program

• Responsible for the high quality of all project deliverables, holding partners, and providers accountable for the quality of their deliverable and/or technical subject matter expert for aspect(s) of the TA, Project, or function

• Leading or contributing to cross-functional administrative or process improvement initiative(s)

• Driving the development of best practices to improve quality, efficiency, and/or effectiveness within the function

• Driving standards development and implementation

• Managing and escalating risk in complicated or novel situations within study and/or projects

• Providing programming expertise to the team

• Providing tactical inputs and/or driving ideas and improvements

• Contributing to the function by supporting recruiting and/or providing training and mentorship

• Identifying opportunities to improve methodology and provides practical solutions for problems

• Managing activities of our external partners (i.e. Contract Research Organisations)

• Influencing stakeholders by providing subject matter expertise on programming related items

• Ensuring compliance to standards and automation usage

• Employing all project management practices in managing drug or technical projects

• Providing input to capacity management for all projects in scope

• Maintaining expertise of the latest industry and regulatory requirements to stay current

Education, Qualifications, Skills, and Experience:

• Degree in Mathematics (i.e., Applied Math, Engineering, etc), Statistics, Computer Science, Life Science, or equivalent

• Excellent programming skills in SAS (or R) and SAS macros

• Thorough knowledge of the clinical development process

• Thorough knowledge of industry standards (CDISC) and ability to implement them

• Ability to apply programming expertise to problem solving and troubleshooting for teams

• Current knowledge of technical and regulatory requirements relevant for the role

• Ability to proactively manage concurrent activities within a project

• Proficient ability to influence relevant stakeholders on programming related items

• Ability to manage risk in complicated or novel situations

• Project Mindset

Desirable Skills/Experience:

• Broad experience across multiple therapeutic areas and across all phases of clinical trials

• Experience in regulatory submissions and interactions

At AstraZeneca, we believe in the potential of our people, and you will develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us. As a Statistical Programming Associate Director, you will play a pivotal role in making a positive impact on changing patients’ lives.

This role is an office-based role with some degree of flexibility. Our vibrant office sites provide a diverse and collaborative work environment, where interactions lead to ideas and innovations, giving you and others the perfect opportunity to learn, grow and develop careers.

Are you ready to bring new ideas and fresh thinking to the table? Apply today!

Date Posted

Closing Date

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.