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ABOUT DEPARTMENT The Trial Safety Review Center (TRISARC) is a department in the Research and Development function of AstraZeneca. The primary remit of the TRISARC is to review large amounts of clinical (mainly safety) data flowing through the clinical trial environment in order to ensure patient data is complete and medically accurate...

At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe. Our dedication to sustainability is also central to our culture and part of what makes...

The Study Contract Manager (SCM) play an important role in driving the costings and contracts being responsible for negotiation and budgeting in clinical trials and for developing and managing contracts and annexes with investigators and institutions or external vendors ensuring ethical, fair and compliant practices.

Innovative, dynamic, and sustainable: As one of the world’s leading research-based pharmaceutical companies, we at AstraZeneca offer the best opportunities for your personal and professional development. For us, it’s clear: when we see a chance for change, we seize it and make it happen.

The Associate Director Clinical Research (ADCR) is responsible for delivering the committed part of all clinical interventional studies under their supervision according to agreed resources, and timelines complying with AZ Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations.

Typically works independently with only moderate supervision and guidance in own knowledge area. Researches and analyses internal and external information to determine methodology choices. Is able to resolve complex issues within specialised area and participates in research projects.

Supplier Excellence Director Location: Warsaw Hybrid Model: 3 days per week from office At AstraZeneca, we are united by a mission to push scientific boundaries and deliver life‑changing medicines. Every colleague plays a vital role in making a real difference for patients worldwide.

You Will: • Formulation and process development, product integration, and manufacturing of patient-centered, unique injectable drug products for Alexion's diverse portfolio from pre-clinical to successful licensure. • Lead interface with Operations, CMC Project management, Clinical Development, Regulatory on life cycle management...

The International Regulatory Affairs Director (IRAD) is responsible for developing and implementing the international regulatory strategy for a group of products. This role ensures that the strategy is designed to achieve rapid approval with advantageous labeling, aligning with the product properties and the needs identified by the...

Global Head of Early Careers and Learning, BioPharma R&D Location: Boston, USA Hybrid Model: minimum 3 days from office in Boston per week Position Overview AstraZeneca is seeking a senior leader to lead Early Careers and Learning in BioPharma R&D.

At AstraZeneca, we turn ideas into life-changing medicines. Working here means thinking big and working together to make the impossible a reality. We’re focused on the potential of science to address the unmet needs of patients around the world. We commit to those areas where we think we can really change the course of medicine and...

Location: Warsaw, Poland Hybrid model of work: 3 days in office, 2 remote per week Human Biological Samples (HBS) are fundamental to medical research in the discovery, development and implementation of new treatments and diagnostics. HBS are ethically sensitive materials, and the collection, handling and access to HBS are subject...

Introduction to role: Join AstraZeneca, a global leader in biopharmaceutical innovation, where science meets passion to create transformative medicines. Our Immunology Cell Therapy Discovery team is on a mission to develop groundbreaking cell therapies that combat and potentially cure immunological diseases.

The International Regulatory Affairs Director (IRAD) is responsible for developing and implementing the international regulatory strategy for a group of products. This role ensures that the strategy is designed to achieve rapid approval with advantageous labelling, aligning with the product properties and the needs identified by the...

Not everyone can claim to feed the world, but it is part of our every day. Behind everything we do for our farmers, there is one AGCO team making it happen. We are proud to put our curiosity into work, building a better and more sustainable world. Join our extraordinary team today! Product development activities considering the legal...

AGCO Power Oy hakee Parts Master Data tiimiin toistaiseksi voimassa olevaan työsuhteeseen Master Data Management Specialistia Tehtävänäsi on luoda ja ylläpitää moottoreiden sekä varaosien tuotetietoja. Osallistut myös erilaisiin varaosiin liittyviin määrittely- ja analysointitehtäviin.

Do you want to help solve the world's most pressing challenges? Feeding the world's growing population and slowing climate change are two of the world's greatest challenges. AGCO is a part of the solution! Join us to make your contribution.

Do you want to help solve the world's most pressing challenges? Feeding the world's growing population and slowing climate change are two of the world's greatest challenges. AGCO is a part of the solution! Join us to make your contribution.

Do you want to help solve the world's most pressing challenges? Feeding the world's growing population and slowing climate change are two of the world's greatest challenges. AGCO is a part of the solution! Join us to make your contribution.

General Summary Join our team as a key craftsperson in bringing each shoe to life. This position plays a hands-on role in shaping footwear on the last, transforming raw components into beautifully structured, expertly crafted shoes. You’ll use traditional skills, technical precision, and an eye for detail to ensure every pair meets...